Map kinase phosphatases and polynucleotides encoding them

ABSTRACT

Novel polynucleotides and the proteins encoded thereby are disclosed.

This application is a continuation-in-part of the following applications:

(1) provisional application Ser. No. 60/075,118, filed Feb. 11, 1998, now abandoned;

(2) application Ser. No. 09/248,059, filed Feb. 10, 1999 (now abandoned); which is a continuation-in-part of provisional application Ser. No. 60/075,118, filed Feb. 11, 1998, now abandoned;

(3) provisional application Ser. No. 60/080,969, filed Apr. 7, 1998, now abandoned;

(4) application Ser. No. 09/287,150, filed Apr. 6, 1999 (now abandoned); which is a continuation-in-part of provisional application Ser. No. 60/080,969, filed Apr. 7, 1998, now abandoned;

(5) provisional application Ser. No. 60/085,472, filed May 14, 1998;

(6) provisional application Ser. No. 60/096,824, filed Aug. 17, 1998;

(7) provisional application Ser. No. 60/099,950, filed Sep. 11, 1998;

(8) provisional application Ser. No. 60/099,843, filed Sep. 11, 1998;

(9) provisional application Ser. No. 60/100,424, filed Sep. 15, 1998;

(10) provisional application Ser. No. 60/102,329, filed Sep. 29, 1998;

(11) provisional application Ser. No. 60/103,615, filed Oct. 9, 1998;

(12) provisional application Ser. No. 60/111,799, filed Dec. 11, 1998;

(13) provisional application Ser. No. 60/112,159, filed Dec. 14, 1998;

(14) provisional application Ser. No. 60/114,415, filed Dec. 31, 1998;

all of which are incorporated by reference herein.

FIELD OF THE INVENTION

The present invention provides novel polynucleotides and proteins encoded by such polynucleotides, along with therapeutic, diagnostic and research utilities for these polynucleotides and proteins.

BACKGROUND OF THE INVENTION

Technology aimed at the discovery of protein factors (including e.g., cytokines, such as lymphokines, interferons, CSFs and interleukins) has matured rapidly over the past decade. The now routine hybridization cloning and expression cloning techniques clone novel polynucleotides “directly” in the sense that they rely on information directly related to the discovered protein (i.e., partial DNA/amino acid sequence of the protein in the case of hybridization cloning; activity of the protein in the case of expression cloning). More recent “indirect” cloning techniques such as signal sequence cloning, which isolates DNA sequences based on the presence of a now well-recognized secretory leader sequence motif, as well as various PCR-based or low stringency hybridization cloning techniques, have advanced the state of the art by making available large numbers of DNA/amino acid sequences for proteins that are known to have biological activity by virtue of their secreted nature in the case of leader sequence cloning, or by virtue of the cell or tissue source in the case of PCR-based techniques. It is to these proteins and the polynucleotides encoding them that the present invention is directed.

SUMMARY OF THE INVENTION

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:1;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:1 from nucleotide 29 to nucleotide 253;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya15_(—)1 deposited under accession number ATCC 98650;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya15_(—)1 deposited under accession number ATCC 98650;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya15_(—)1 deposited under accession number ATCC 98650;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya15_(—)1 deposited under accession number ATCC 98650;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:2;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:2;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:1.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:1 from nucleotide 29 to nucleotide 253; the nucleotide sequence of the full-length protein coding sequence of clone ya15_(—)1 deposited under accession number ATCC 98650; or the nucleotide sequence of a mature protein coding sequence of clone ya15_(—)1 deposited under accession number ATCC 98650. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya15_(—)1 deposited under accession number ATCC 98650. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:2, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment comprising the amino acid sequence from amino acid 32 to amino acid 41 of SEQ ID NO:2.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:1.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:1, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:1; and

(ab) the nucleotide sequence of the cDNA insert of clone ya15_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:1, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:1; and

(bb) the nucleotide sequence of the cDNA insert of clone ya15_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:1, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:1 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:1, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:1. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:1 from nucleotide 29 to nucleotide 253, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:1 from nucleotide 29 to nucleotide 253, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:1 from nucleotide 29 to nucleotide 253.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:2;

(b) a fragment of the amino acid sequence of SEQ ID NO:2, the fragment comprising eight contiguous amino acids of SEQ ID NO:2; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya15_(—)1 deposited under accession number ATCC 98650;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:2. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:2, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:2 having biological activity, the fragment comprising the amino acid sequence from amino acid 32 to amino acid 41 of SEQ ID NO:2.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:3;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:3 from nucleotide 151 to nucleotide 288;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:3 from nucleotide 196 to nucleotide 288;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya24_(—)1 deposited under accession number ATCC 98650;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya24_(—)1 deposited under accession number ATCC 98650;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya24_(—)1 deposited under accession number ATCC 98650;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya24_(—)1 deposited under accession number ATCC 98650;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:4;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:4;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:3.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:3 from nucleotide 151 to nucleotide 288; the nucleotide sequence of SEQ ID NO:3 from nucleotide 196 to nucleotide 288; the nucleotide sequence of the full-length protein coding sequence of clone ya24_(—)1 deposited under accession number ATCC 98650; or the nucleotide sequence of a mature protein coding sequence of clone ya24_(—)1 deposited under accession number ATCC 98650. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya24_(—)1 deposited under accession number ATCC 98650. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:4, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment comprising the amino acid sequence from amino acid 18 to amino acid 27 of SEQ ID NO:4.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:3.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:3, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:3; and

(ab) the nucleotide sequence of the cDNA insert of clone ya24_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:3, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:3; and

(bb) the nucleotide sequence of the cDNA insert of clone ya24_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:3, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:3 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:3, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:3. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:3 from nucleotide 151 to nucleotide 288, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:3 from nucleotide 151 to nucleotide 288, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:3 from nucleotide 151 to nucleotide 288. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:3 from nucleotide 196 to nucleotide 288, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:3 from nucleotide 196 to nucleotide 288, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:3 from nucleotide 196 to nucleotide 288.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:4;

(b) a fragment of the amino acid sequence of SEQ ID NO:4, the fragment comprising eight contiguous amino acids of SEQ ID NO:4; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya24_(—)1 deposited under accession number ATCC 98650;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:4. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:4, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:4 having biological activity, the fragment comprising the amino acid sequence from amino acid 18 to amino acid 27 of SEQ ID NO:4.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5 from nucleotide 615 to nucleotide 908;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5 from nucleotide 774 to nucleotide 908;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb42_(—)1 deposited under accession number ATCC 98650;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb42_(—)1 deposited under accession number ATCC 98650;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb42_(—)1 deposited under accession number ATCC 98650;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb42_(—)1 deposited under accession number ATCC 98650;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:6;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:6;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:5.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:5 from nucleotide 615 to nucleotide 908; the nucleotide sequence of SEQ ID NO:5 from nucleotide 774 to nucleotide 908; the nucleotide sequence of the full-length protein coding sequence of clone yb42_(—)1 deposited under accession number ATCC 98650; or the nucleotide sequence of a mature protein coding sequence of clone yb42_(—)1 deposited under accession number ATCC 98650. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb42_(—)1 deposited under accession number ATCC 98650. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:6, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:6.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:5.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:5, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:5; and

(ab) the nucleotide sequence of the cDNA insert of clone yb42_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:5, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:5; and

(bb) the nucleotide sequence of the cDNA insert of clone yb42_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:5, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:5 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:5, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:5. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:5 from nucleotide 615 to nucleotide 908, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:5 from nucleotide 615 to nucleotide 908, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:5 from nucleotide 615 to nucleotide 908. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:5 from nucleotide 774 to nucleotide 908, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:5 from nucleotide 774 to nucleotide 908, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:5 from nucleotide 774 to nucleotide 908.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:6;

(b) a fragment of the amino acid sequence of SEQ ID NO:6, the fragment comprising eight contiguous amino acids of SEQ ID NO:6; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb42_(—)1 deposited under accession number ATCC 98650;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:6. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:6, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:6 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:6.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:7;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:7 from nucleotide 1203 to nucleotide 2327;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc9_(—)1 deposited under accession number ATCC 98650;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc9_(—)1 deposited under accession number ATCC 98650;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc9_(—)1 deposited under accession number ATCC 98650;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc9_(—)1 deposited under accession number ATCC 98650;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:8;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:8;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:7.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:7 from nucleotide 1203 to nucleotide 2327; the nucleotide sequence of the full-length protein coding sequence of clone yc9_(—)1 deposited under accession number ATCC 98650; or the nucleotide sequence of a mature protein coding sequence of clone yc9_(—)1 deposited under accession number ATCC 98650. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc9_(—)1 deposited under accession number ATCC 98650. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:8, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment comprising the amino acid sequence from amino acid 182 to amino acid 191 of SEQ ID NO:8.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:7.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:7, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:7; and

(ab) the nucleotide sequence of the cDNA insert of clone yc9_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:7, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:7; and

(bb) the nucleotide sequence of the cDNA insert of clone yc9_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:7, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:7 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:7, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:7. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:7 from nucleotide 1203 to nucleotide 2327, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:7 from nucleotide 1203 to nucleotide 2327, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:7 from nucleotide 1203 to nucleotide 2327.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:8;

(b) a fragment of the amino acid sequence of SEQ ID NO:8, the fragment comprising eight contiguous amino acids of SEQ ID NO:8; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc9_(—)1 deposited under accession number ATCC 98650;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:8. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:8, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:8 having biological activity, the fragment comprising the amino acid sequence from amino acid 182 to amino acid 191 of SEQ ID NO:8.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:9;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:9 from nucleotide 230 to nucleotide 823;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:9 from nucleotide 584 to nucleotide 823;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc19_(—)1 deposited under accession number ATCC 98650;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc19_(—)1 deposited under accession number ATCC 98650;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc19_(—)1 deposited under accession number ATCC 98650;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc19_(—)1 deposited under accession number ATCC 98650;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:10;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:10 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:10;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:9.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:9 from nucleotide 230 to nucleotide 823; the nucleotide sequence of SEQ ID NO:9 from nucleotide 584 to nucleotide 823; the nucleotide sequence of the full-length protein coding sequence of clone yc19_(—)1 deposited under accession number ATCC 98650; or the nucleotide sequence of a mature protein coding sequence of clone yc19_(—)1 deposited under accession number ATCC 98650. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc19_(—)1 deposited under accession number ATCC 98650. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:10 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:10, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:10 having biological activity, the fragment comprising the amino acid sequence from amino acid 94 to amino acid 103 of SEQ ID NO:10.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:9.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:9, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:9; and

(ab) the nucleotide sequence of the cDNA insert of clone yc19_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:9, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:9; and

(bb) the nucleotide sequence of the cDNA insert of clone yc19_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:9, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:9 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:9, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:9. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:9 from nucleotide 230 to nucleotide 823, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:9 from nucleotide 230 to nucleotide 823, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:9 from nucleotide 230 to nucleotide 823. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:9 from nucleotide 584 to nucleotide 823, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:9 from nucleotide 584 to nucleotide 823, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:9 from nucleotide 584 to nucleotide 823.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:10;

(b) a fragment of the amino acid sequence of SEQ ID NO:10, the fragment comprising eight contiguous amino acids of SEQ ID NO:10; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc19_(—)1 deposited under accession number ATCC 98650;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:10. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:10 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:10, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:10 having biological activity, the fragment comprising the amino acid sequence from amino acid 94 to amino acid 103 of SEQ ID NO:10.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:11;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:11 from nucleotide 292 to nucleotide 534;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc20_(—)1 deposited under accession number ATCC 98650;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc20_(—)1 deposited under accession number ATCC 98650;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc20_(—)1 deposited under accession number ATCC 98650;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc20_(—)1 deposited under accession number ATCC 98650;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:12;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:12;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:11.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:11 from nucleotide 292 to nucleotide 534; the nucleotide sequence of the full-length protein coding sequence of clone yc20_(—)1 deposited under accession number ATCC 98650; or the nucleotide sequence of a mature protein coding sequence of clone yc20_(—)1 deposited under accession number ATCC 98650. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc20_(—)1 deposited under accession number ATCC 98650. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:12, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment comprising the amino acid sequence from amino acid 35 to amino acid 44 of SEQ ID NO:12.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:11.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:11, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:11; and

(ab) the nucleotide sequence of the cDNA insert of clone yc20_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:11, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:11; and

(bb) the nucleotide sequence of the cDNA insert of clone yc20_(—)1 deposited under accession number ATCC 98650;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:11, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:11 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:11, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:11. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:11 from nucleotide 292 to nucleotide 534, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:11 from nucleotide 292 to nucleotide 534, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:11 from nucleotide 292 to nucleotide 534.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:12;

(b) a fragment of the amino acid sequence of SEQ ID NO:12, the fragment comprising eight contiguous amino acids of SEQ ID NO:12; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc20_(—)1 deposited under accession number ATCC 98650;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:12. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:12, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:12 having biological activity, the fragment comprising the amino acid sequence from amino acid 35 to amino acid 44 of SEQ ID NO:12.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:13;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:13 from nucleotide 45 to nucleotide 590;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:13 from nucleotide 126 to nucleotide 590;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya9_(—)1 deposited under accession number ATCC 98724;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya9_(—)1 deposited under accession number ATCC 98724;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya9_(—)1 deposited under accession number ATCC 98724;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya9_(—)1 deposited under accession number ATCC 98724;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:14;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:14;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:13.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:13 from nucleotide 45 to nucleotide 590; the nucleotide sequence of SEQ ID NO:13 from nucleotide 126 to nucleotide 590; the nucleotide sequence of the full-length protein coding sequence of clone ya9_(—)1 deposited under accession number ATCC 98724; or the nucleotide sequence of a mature protein coding sequence of clone ya9_(—)1 deposited under accession number ATCC 98724. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya9_(—)1 deposited under accession number ATCC 98724. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:14, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment comprising the amino acid sequence from amino acid 86 to amino acid 95 of SEQ ID NO:14.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:13.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:13, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:13; and

(ab) the nucleotide sequence of the cDNA insert of clone ya9_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:13, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:13; and

(bb) the nucleotide sequence of the cDNA insert of clone ya9_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:13, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:13 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:13, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:13. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:13 from nucleotide 45 to nucleotide 590, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:13 from nucleotide 45 to nucleotide 590, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:13 from nucleotide 45 to nucleotide 590. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:13 from nucleotide 126 to nucleotide 590, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:13 from nucleotide 126 to nucleotide 590, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:13 from nucleotide 126 to nucleotide 590.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino add sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:14;

(b) a fragment of the amino acid sequence of SEQ ID NO:14, the fragment comprising eight contiguous amino acids of SEQ ID NO:14; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya9_(—)1 deposited under accession number ATCC 98724;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:14. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:14, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:14 having biological activity, the fragment comprising the amino acid sequence from amino acid 86 to amino acid 95 of SEQ ID NO:14.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:15;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:15 from nucleotide 194 to nucleotide 466;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:15 from nucleotide 338 to nucleotide 466;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya11_(—)1 deposited under accession number ATCC 98724;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya11_(—)1 deposited under accession number ATCC 98724;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya11_(—)1 deposited under accession number ATCC 98724;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya11_(—)1 deposited under accession number ATCC 98724;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:16;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:16;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:15.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:15 from nucleotide 194 to nucleotide 466; the nucleotide sequence of SEQ ID NO:15 from nucleotide 338 to nucleotide 466; the nucleotide sequence of the full-length protein coding sequence of clone ya11_(—)1 deposited under accession number ATCC 98724; or the nucleotide sequence of a mature protein coding sequence of clone ya11_(—)1 deposited under accession number ATCC 98724. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya11_(—)1 deposited under accession number ATCC 98724. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:16, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:16.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:15.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:15, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:15; and

(ab) the nucleotide sequence of the cDNA insert of clone ya11_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:15, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:15; and

(bb) the nucleotide sequence of the cDNA insert of clone ya11_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:15, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:15 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:15, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:15. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:15 from nucleotide 194 to nucleotide 466, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:15 from nucleotide 194 to nucleotide 466, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:15 from nucleotide 194 to nucleotide 466. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:15 from nucleotide 338 to nucleotide 466, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:15 from nucleotide 338 to nucleotide 466, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:15 from nucleotide 338 to nucleotide 466.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:16;

(b) a fragment of the amino acid sequence of SEQ ID NO:16, the fragment comprising eight contiguous amino acids of SEQ ID NO:16; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya11_(—)1 deposited under accession number ATCC 98724;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:16. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:16, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:16 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:16.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:17;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:17 from nucleotide 15 to nucleotide 233;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:17 from nucleotide 174 to nucleotide 233;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya28_(—)1 deposited under accession number ATCC 98724;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya28_(—)1 deposited under accession number ATCC 98724;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya28_(—)1 deposited under accession number ATCC 98724;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya28_(—)1 deposited under accession number ATCC 98724;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:18;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:18;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:17.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:17 from nucleotide 15 to nucleotide 233; the nucleotide sequence of SEQ ID NO:17 from nucleotide 174 to nucleotide 233; the nucleotide sequence of the full-length protein coding sequence of clone ya28_(—)1 deposited under accession number ATCC 98724; or the nucleotide sequence of a mature protein coding sequence of clone ya28_(—)1 deposited under accession number ATCC 98724. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya28_(—)1 deposited under accession number ATCC 98724. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:18, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment comprising the amino acid sequence from amino acid 31 to amino acid 40 of SEQ ID NO:18.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:17.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:17, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:17; and

(ab) the nucleotide sequence of the cDNA insert of clone ya28_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:17, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:17; and

(bb) the nucleotide sequence of the cDNA insert of clone ya28_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:17, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:17 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:17, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:17. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:17 from nucleotide 15 to nucleotide 233, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:17 from nucleotide 15 to nucleotide 233, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:17 from nucleotide 15 to nucleotide 233. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:17 from nucleotide 174 to nucleotide 233, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:17 from nucleotide 174 to nucleotide 233, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:17 from nucleotide 174 to nucleotide 233.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:18;

(b) a fragment of the amino acid sequence of SEQ ID NO:18, the fragment comprising eight contiguous amino acids of SEQ ID NO:18; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya28_(—)1 deposited under accession number ATCC 98724;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:18. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:18, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:18 having biological activity, the fragment comprising the amino acid sequence from amino acid 31 to amino acid 40 of SEQ ID NO:18.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:19;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:19 from nucleotide 102 to nucleotide 461;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb81_(—)1 deposited under accession number ATCC 98724;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb81_(—)1 deposited under accession number ATCC 98724;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb81_(—)1 deposited under accession number ATCC 98724;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb81_(—)1 deposited under accession number ATCC 98724;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:20;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:20;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:19.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:19 from nucleotide 102 to nucleotide 461; the nucleotide sequence of the full-length protein coding sequence of clone yb81l1 deposited under accession number ATCC 98724; or the nucleotide sequence of a mature protein coding sequence of clone yb81l1 deposited under accession number ATCC 98724. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb81_(—)1 deposited under accession number ATCC 98724. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:20, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment comprising the amino acid sequence from amino acid 55 to amino acid 64 of SEQ ID NO:20.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:19.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:19, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:19; and

(ab) the nucleotide sequence of the cDNA insert of clone yb81_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:19, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:19; and

(bb) the nucleotide sequence of the cDNA insert of clone yb811 deposited under accession number ATCC 98724;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:19, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:19 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:19, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:19. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:19 from nucleotide 102 to nucleotide 461, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:19 from nucleotide 102 to nucleotide 461, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:19 from nucleotide 102 to nucleotide 461.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:20;

(b) a fragment of the amino acid sequence of SEQ ID NO:20, the fragment comprising eight contiguous amino acids of SEQ ID NO:20; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb81_(—)1 deposited under accession number ATCC 98724;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:20. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:20, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:20 having biological activity, the fragment comprising the amino acid sequence from amino acid 55 to amino acid 64 of SEQ ID NO:20.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:21;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:21 from nucleotide 170 to nucleotide 2968;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc14_(—)1 deposited under accession number ATCC 98724;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc14_(—)1 deposited under accession number ATCC 98724;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc14_(—)1 deposited under accession number ATCC 98724;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc14_(—)1 deposited under accession number ATCC 98724;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:22;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:22 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:22;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:21.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:21 from nucleotide 170 to nucleotide 2968; the nucleotide sequence of the full-length protein coding sequence of clone yc14_(—)1 deposited under accession number ATCC 98724; or the nucleotide sequence of a mature protein coding sequence of clone yc14_(—)1 deposited under accession number ATCC 98724. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc14_(—)1 deposited under accession number ATCC 98724. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:22 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:22, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:22 having biological activity, the fragment comprising the amino acid sequence from amino acid 461 to amino acid 470 of SEQ ID NO:22.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:21.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:21, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:21; and

(ab) the nucleotide sequence of the cDNA insert of clone yc14_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:21, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:21; and

(bb) the nucleotide sequence of the cDNA insert of done yc14_(—)1 deposited under accession number ATCC 98724;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:21, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:21 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:21, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:21. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:21 from nucleotide 170 to nucleotide 2968, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:21 from nucleotide 170 to nucleotide 2968, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:21 from nucleotide 170 to nucleotide 2968.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:22;

(b) a fragment of the amino acid sequence of SEQ ID NO:22, the fragment comprising eight contiguous amino acids of SEQ ID NO:22; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc14_(—)1 deposited under accession number ATCC 98724;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:22. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:22 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:22, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:22 having biological activity, the fragment comprising the amino acid sequence from amino acid 461 to amino acid 470 of SEQ ID NO:22.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:23;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:23 from nucleotide 82 to nucleotide 729;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc24_(—)1 deposited under accession number ATCC 98755;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc24_(—)1 deposited under accession number ATCC 98755;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc24_(—)1 deposited under accession number ATCC 98755;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc24_(—)1 deposited under accession number ATCC 98755;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:24;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:24 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:24;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:23.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:23 from nucleotide 82 to nucleotide 729; the nucleotide sequence of the full-length protein coding sequence of clone yc24_(—)1 deposited under accession number ATCC 98755; or the nucleotide sequence of a mature protein coding sequence of clone yc24_(—)1 deposited under accession number ATCC 98755. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc24_(—)1 deposited under accession number ATCC 98755. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:24 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:24, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:24 having biological activity, the fragment comprising the amino acid sequence from amino acid 103 to amino acid 112 of SEQ ID NO:24.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:23.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:23, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:23; and

(ab) the nucleotide sequence of the cDNA insert of clone yc24_(—)1 deposited under accession number ATCC 98755;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:23, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:23; and

(bb) the nucleotide sequence of the cDNA insert of clone yc24_(—)1 deposited under accession number ATCC 98755;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:23, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:23 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:23, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:23. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:23 from nucleotide 82 to nucleotide 729, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:23 from nucleotide 82 to nucleotide 729, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:23 from nucleotide 82 to nucleotide 729.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:24;

(b) a fragment of the amino acid sequence of SEQ ID NO:24, the fragment comprising eight contiguous amino acids of SEQ ID NO:24; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc24_(—)1 deposited under accession number ATCC 98755;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:24. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:24 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:24, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:24 having biological activity, the fragment comprising the amino acid sequence from amino acid 103 to amino acid 112 of SEQ ID NO:24.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:25;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:25 from nucleotide 7 to nucleotide 951;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:25 from nucleotide 61 to nucleotide 951;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc25_(—)1 deposited under accession number ATCC 98755;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc25_(—)1 deposited under accession number ATCC 98755;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc25_(—)1 deposited under accession number ATCC 98755;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc25_(—)1 deposited under accession number ATCC 98755;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:26;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:26 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:26;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:25.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:25 from nucleotide 7 to nucleotide 951; the nucleotide sequence of SEQ ID NO:25 from nucleotide 61 to nucleotide 951; the nucleotide sequence of the full-length protein coding sequence of clone yc25_(—)1 deposited under accession number ATCC 98755; or the nucleotide sequence of a mature protein coding sequence of clone yc25_(—)1 deposited under accession number ATCC 98755. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc25_(—)1 deposited under accession number ATCC 98755. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:26 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:26, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:26 having biological activity, the fragment comprising the amino acid sequence from amino acid 152 to amino acid 161 of SEQ ID NO:26.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:25.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:25, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:25; and

(ab) the nucleotide sequence of the cDNA insert of clone yc25_(—)1 deposited under accession number ATCC 98755;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:25, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:25; and

(bb) the nucleotide sequence of the cDNA insert of clone yc25_(—)1 deposited under accession number ATCC 98755;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:25, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:25 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:25, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:25. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:25 from nucleotide 7 to nucleotide 951, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:25 from nucleotide 7 to nucleotide 951, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:25 from nucleotide 7 to nucleotide 951. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:25 from nucleotide 61 to nucleotide 951, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:25 from nucleotide 61 to nucleotide 951, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:25 from nucleotide 61 to nucleotide 951.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:26;

(b) a fragment of the amino acid sequence of SEQ ID NO:26, the fragment comprising eight contiguous amino acids of SEQ ID NO:26; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc25_(—)1 deposited under accession number ATCC 98755;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:26. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:26 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:26, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:26 having biological activity, the fragment comprising the amino acid sequence from amino acid 152 to amino acid 161 of SEQ ID NO:26.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:27;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:27 from nucleotide 157 to nucleotide 1083;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye2_(—)1 deposited under accession number ATCC 98755;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye2_(—)1 deposited under accession number ATCC 98755;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye2_(—)1 deposited under accession number ATCC 98755;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye2_(—)1 deposited under accession number ATCC 98755;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:28;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:28 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:28;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:27.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:27 from nucleotide 157 to nucleotide 1083; the nucleotide sequence of the full-length protein coding sequence of clone ye2_(—)1 deposited under accession number ATCC 98755; or the nucleotide sequence of a mature protein coding sequence of clone ye2_(—)1 deposited under accession number ATCC 98755. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye2_(—)1 deposited under accession number ATCC 98755. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:28 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:28, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:28 having biological activity, the fragment comprising the amino acid sequence from amino acid 149 to amino acid 158 of SEQ ID NO:28.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:27.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:27, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:27; and

(ab) the nucleotide sequence of the cDNA insert of clone ye2_(—)1 deposited under accession number ATCC 98755;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:27, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:27; and

(bb) the nucleotide sequence of the cDNA insert of clone ye2_(—)1 deposited under accession number ATCC 98755;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:27, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:27 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:27, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:27. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:27 from nucleotide 157 to nucleotide 1083, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:27 from nucleotide 157 to nucleotide 1083, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:27 from nucleotide 157 to nucleotide 1083.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:28;

(b) a fragment of the amino acid sequence of SEQ ID NO:28, the fragment comprising eight contiguous amino acids of SEQ ID NO:28; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye2_(—)1 deposited under accession number ATCC 98755;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:28. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:28 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:28, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:28 having biological activity, the fragment comprising the amino acid sequence from amino acid 149 to amino acid 158 of SEQ ID NO:28.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:29;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:29 from nucleotide 39 to nucleotide 473;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya65_(—)1 deposited under accession number ATCC 98834;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya65_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya65_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya65_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:30;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:30 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:30;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:29.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:29 from nucleotide 39 to nucleotide 473; the nucleotide sequence of the full-length protein coding sequence of clone ya65_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone ya65_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya65_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:30 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:30, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:30 having biological activity, the fragment comprising the amino acid sequence from amino acid 67 to amino acid 76 of SEQ ID NO:30.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:29.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:29, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:29; and

(ab) the nucleotide sequence of the cDNA insert of clone ya65_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:29, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:29; and

(bb) the nucleotide sequence of the cDNA insert of clone ya65_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:29, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:29 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:29, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:29. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:29 from nucleotide 39 to nucleotide 473, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:29 from nucleotide 39 to nucleotide 473, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:29 from nucleotide 39 to nucleotide 473.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:30;

(b) a fragment of the amino acid sequence of SEQ ID NO:30, the fragment comprising eight contiguous amino acids of SEQ ID NO:30; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya65_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:30. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:30 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:30, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:30 having biological activity, the fragment comprising the amino acid sequence from amino acid 67 to amino acid 76 of SEQ ID NO:30.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:31;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:31 from nucleotide 664 to nucleotide 903;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb60_(—)1 deposited under accession number ATCC 98834;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb60_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb60_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb60_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:32;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:32 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:32;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:31.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:31 from nucleotide 664 to nucleotide 903; the nucleotide sequence of the full-length protein coding sequence of clone yb60_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone yb60_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb60_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:32 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:32, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:32 having biological activity, the fragment comprising the amino acid sequence from amino acid 35 to amino acid 44 of SEQ ID NO:32.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:31.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:31, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:31; and

(ab) the nucleotide sequence of the cDNA insert of clone yb60_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:31, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:31; and

(bb) the nucleotide sequence of the cDNA insert of clone yb60_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:31, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:31 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:31, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:31. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:31 from nucleotide 664 to nucleotide 903, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:31 from nucleotide 664 to nucleotide 903, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:31 from nucleotide 664 to nucleotide 903.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:32;

(b) a fragment of the amino acid sequence of SEQ ID NO:32, the fragment comprising eight contiguous amino acids of SEQ ID NO:32; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb60_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:32. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:32 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:32, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:32 having biological activity, the fragment comprising the amino acid sequence from amino acid 35 to amino acid 44 of SEQ ID NO:32.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:33;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:33 from nucleotide 88 to nucleotide 447;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:33 from nucleotide 427 to nucleotide 447;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb139_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb139_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb139_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb139_(—)1 deposited under accession number ATCC 98834;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:34;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:34 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:34;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:33.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:33 from nucleotide 88 to nucleotide 447; the nucleotide sequence of SEQ ID NO:33 from nucleotide 427 to nucleotide 447; the nucleotide sequence of the full-length protein coding sequence of clone yb139_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone yb139_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb139_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:34 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:34, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:34 having biological activity, the fragment comprising the amino acid sequence from amino acid 55 to amino acid 64 of SEQ ID NO:34.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:33.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:33, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:33; and

(ab) the nucleotide sequence of the cDNA insert of clone yb139_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:33, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:33; and

(bb) the nucleotide sequence of the cDNA insert of clone yb139_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:33, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:33 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:33, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:33. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:33 from nucleotide 88 to nucleotide 447, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:33 from nucleotide 88 to nucleotide 447, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:33 from nucleotide 88 to nucleotide 447. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:33 from nucleotide 427 to nucleotide 447, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:33 from nucleotide 427 to nucleotide 447, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:33 from nucleotide 427 to nucleotide 447.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:34;

(b) a fragment of the amino acid sequence of SEQ ID NO:34, the fragment comprising eight contiguous amino acids of SEQ ID NO:34; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb139_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:34. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:34 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:34, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:34 having biological activity, the fragment comprising the amino acid sequence from amino acid 55 to amino acid 64 of SEQ ID NO:34.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:35;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:35 from nucleotide 93 to nucleotide 1481;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc29_(—)1 deposited under accession number ATCC 98834;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc29_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc29_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc29_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:36;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:36 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:36;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:35.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:35 from nucleotide 93 to nucleotide 1481; the nucleotide sequence of the full-length protein coding sequence of done yc29_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone yc29_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc29_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:36 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:36, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:36 having biological activity, the fragment comprising the amino acid sequence from amino acid 226 to amino acid 235 of SEQ ID NO:36.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:35.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:35, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:35; and

(ab) the nucleotide sequence of the cDNA insert of clone yc29_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:35, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:35; and

(bb) the nucleotide sequence of the cDNA insert of clone yc29_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:35, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:35 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:35, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:35. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:35 from nucleotide 93 to nucleotide 1481, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:35 from nucleotide 93 to nucleotide 1481, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:35 from nucleotide 93 to nucleotide 1481.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:36;

(b) a fragment of the amino acid sequence of SEQ ID NO:36, the fragment comprising eight contiguous amino acids of SEQ ID NO:36; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc29_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:36. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:36 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:36, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:36 having biological activity, the fragment comprising the amino acid sequence from amino acid 226 to amino acid 235 of SEQ ID NO:36.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:37;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:37 from nucleotide 482 to nucleotide 751;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:37 from nucleotide 611 to nucleotide 751;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc40_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc40_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc40_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc40_(—)1 deposited under accession number ATCC 98834;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:38;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:38 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:38;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:37.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:37 from nucleotide 482 to nucleotide 751; the nucleotide sequence of SEQ ID NO:37 from nucleotide 611 to nucleotide 751; the nucleotide sequence of the full-length protein coding sequence of clone yc40_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone yc40_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc40_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:38 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:38, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:38 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:38.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:37.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:37, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:37; and

(ab) the nucleotide sequence of the cDNA insert of clone yc40_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:37, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:37; and

(bb) the nucleotide sequence of the cDNA insert of clone yc40_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:37, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:37 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:37, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:37. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:37 from nucleotide 482 to nucleotide 751, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:37 from nucleotide 482 to nucleotide 751, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:37 from nucleotide 482 to nucleotide 751. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:37 from nucleotide 611 to nucleotide 751, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:37 from nucleotide 611 to nucleotide 751, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:37 from nucleotide 611 to nucleotide 751.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:38;

(b) a fragment of the amino acid sequence of SEQ ID NO:38, the fragment comprising eight contiguous amino acids of SEQ ID NO:38; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc40_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:38. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:38 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:38, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:38 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:38.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:39;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:39 from nucleotide 179 to nucleotide 601;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:39 from nucleotide 356 to nucleotide 601;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd10_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd10_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd10_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd10_(—)1 deposited under accession number ATCC 98834;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:40;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:40 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:40;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:39.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:39 from nucleotide 179 to nucleotide 601; the nucleotide sequence of SEQ ID NO:39 from nucleotide 356 to nucleotide 601; the nucleotide sequence of the full-length protein coding sequence of clone yd10_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone yd10_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd10_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:40 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:40, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:40 having biological activity, the fragment comprising the amino acid sequence from amino acid 65 to amino acid 74 of SEQ ID NO:40.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:39.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:39, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:39; and

(ab) the nucleotide sequence of the cDNA insert of clone yd10_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:39, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:39; and

(bb) the nucleotide sequence of the cDNA insert of clone yd10_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:39, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:39 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:39, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:39. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:39 from nucleotide 179 to nucleotide 601, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:39 from nucleotide 179 to nucleotide 601, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:39 from nucleotide 179 to nucleotide 601. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:39 from nucleotide 356 to nucleotide 601, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:39 from nucleotide 356 to nucleotide 601, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:39 from nucleotide 356 to nucleotide 601.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:40;

(b) a fragment of the amino acid sequence of SEQ ID NO:40, the fragment comprising eight contiguous amino acids of SEQ ID NO:40; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd10_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:40. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:40 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:40, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:40 having biological activity, the fragment comprising the amino acid sequence from amino acid 65 to amino acid 74 of SEQ ID NO:40.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:41;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:41 from nucleotide 324 to nucleotide 1559;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:41 from nucleotide 387 to nucleotide 1559;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yf5_(—)1 deposited under accession number ATCC 98834;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yf5_(—)1 deposited under accession number ATCC 98834;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yf5_(—)1 deposited under accession number ATCC 98834;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yf5_(—)1 deposited under accession number ATCC 98834;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:42;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:42 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:42;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:41.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:41 from nucleotide 324 to nucleotide 1559; the nucleotide sequence of SEQ ID NO:41 from nucleotide 387 to nucleotide 1559; the nucleotide sequence of the full-length protein coding sequence of clone yf5_(—)1 deposited under accession number ATCC 98834; or the nucleotide sequence of a mature protein coding sequence of clone yf5_(—)1 deposited under accession number ATCC 98834. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yf5_(—)1 deposited under accession number ATCC 98834. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:42 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:42, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:42 having biological activity, the fragment comprising the amino acid sequence from amino acid 201 to amino acid 210 of SEQ ID NO:42.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:41.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:41, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:41; and

(ab) the nucleotide sequence of the cDNA insert of clone yf5_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:41, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:41; and

(bb) the nucleotide sequence of the cDNA insert of clone yf5_(—)1 deposited under accession number ATCC 98834;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:41, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:41 to a nucleotide sequence corresponding to the 3′ end of SEQ ID. NO:41, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:41. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:41 from nucleotide 324 to nucleotide 1559, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:41 from nucleotide 324 to nucleotide 1559, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:41 from nucleotide 324 to nucleotide 1559. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:41 from nucleotide 387 to nucleotide 1559, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:41 from nucleotide 387 to nucleotide 1559, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:41 from nucleotide 387 to nucleotide 1559.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:42;

(b) a fragment of the amino acid sequence of SEQ ID NO:42, the fragment comprising eight contiguous amino acids of SEQ ID NO:42; and

(c) the amino acid sequence encoded by the cDNA insert of clone yf5_(—)1 deposited under accession number ATCC 98834;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:42. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:42 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:42, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:42 having biological activity, the fragment comprising the amino acid sequence from amino acid 201 to amino acid 210 of SEQ ID NO:42.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:43;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:43 from nucleotide 257 to nucleotide 649;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:43 from nucleotide 335 to nucleotide 649;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya67_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya67_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya67_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya67_(—)1 deposited under accession number ATCC 98864;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:44;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:44 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:44;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:43.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:43 from nucleotide 257 to nucleotide 649; the nucleotide sequence of SEQ ID NO:43 from nucleotide 335 to nucleotide 649; the nucleotide sequence of the full-length protein coding sequence of done ya67_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone ya67_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya67_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:44 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:44, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:44 having biological activity, the fragment comprising the amino acid sequence from amino acid 60 to amino acid 69 of SEQ ID NO:44.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:43.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:43, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:43; and

(ab) the nucleotide sequence of the cDNA insert of clone ya67_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:43, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:43; and

(bb) the nucleotide sequence of the cDNA insert of clone ya67_(—)1 deposited under accession number ATCC 98864;

(j) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:43, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:43 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:43, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:43. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:43 from nucleotide 257 to nucleotide 649, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:43 from nucleotide 257 to nucleotide 649, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:43 from nucleotide 257 to nucleotide 649. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:43 from nucleotide 335 to nucleotide 649, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:43 from nucleotide 335 to nucleotide 649, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:43 from nucleotide 335 to nucleotide 649.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:44;

(b) a fragment of the amino acid sequence of SEQ ID NO:44, the fragment comprising eight contiguous amino acids of SEQ ID NO:44; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya67_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:44. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:44 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:44, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:44 having biological activity, the fragment comprising the amino acid sequence from amino acid 60 to amino acid 69 of SEQ ID NO:44.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:45;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:45 from nucleotide 89 to nucleotide 787;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya70_(—)1 deposited under accession number ATCC 98864;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya70_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya70_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya70_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:46;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:46 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:46;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:45.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:45 from nucleotide 89 to nucleotide 787; the nucleotide sequence of the full-length protein coding sequence of clone ya70_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone ya70_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya70_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:46 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:46, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:46 having biological activity, the fragment comprising the amino acid sequence from amino acid 111 to amino acid 120 of SEQ ID NO:46.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:45.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:45, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:45; and

(ab) the nucleotide sequence of the cDNA insert of clone ya70_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:45, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:45; and

(bb) the nucleotide sequence of the cDNA insert of clone ya70_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:45, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:45 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:45, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:45. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:45 from nucleotide 89 to nucleotide 787, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:45 from nucleotide 89 to nucleotide 787, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:45 from nucleotide 89 to nucleotide 787.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:46;

(b) a fragment of the amino acid sequence of SEQ ID NO:46, the fragment comprising eight contiguous amino acids of SEQ ID NO:46; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya70_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:46. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:46 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:46, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:46 having biological activity, the fragment comprising the amino acid sequence from amino acid 111 to amino acid 120 of SEQ ID NO:46.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:47;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:47 from nucleotide 1017 to nucleotide 1265;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:47 from nucleotide 1068 to nucleotide 1265;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb51_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb51_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb51_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb51_(—)1 deposited under accession number ATCC 98864;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:48;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:48 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:48;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:47.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:47 from nucleotide 1017 to nucleotide 1265; the nucleotide sequence of SEQ ID NO:47 from nucleotide 1068 to nucleotide 1265; the nucleotide sequence of the full-length protein coding sequence of clone yb51_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone yb51_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb51_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:48 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:48, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:48 having biological activity, the fragment comprising the amino acid sequence from amino acid 36 to amino acid 45 of SEQ ID NO:48.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:47.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:47, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:47; and

(ab) the nucleotide sequence of the cDNA insert of clone yb51_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:47, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:47; and

(bb) the nucleotide sequence of the cDNA insert of clone yb51_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:47, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:47 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:47, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:47. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:47 from nucleotide 1017 to nucleotide 1265, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:47 from nucleotide 1017 to nucleotide 1265, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:47 from nucleotide 1017 to nucleotide 1265. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:47 from nucleotide 1068 to nucleotide 1265, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:47 from nucleotide 1068 to nucleotide 1265, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:47 from nucleotide 1068 to nucleotide 1265.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:48;

(b) a fragment of the amino acid sequence of SEQ ID NO:48, the fragment comprising eight contiguous amino acids of SEQ ID NO:48; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb51_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:48. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:48 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:48, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:48 having biological activity, the fragment comprising the amino acid sequence from amino acid 36 to amino acid 45 of SEQ ID NO:48.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:49;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:49 from nucleotide 13 to nucleotide 306;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb101_(—)1 deposited under accession number ATCC 98864;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb101_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb101_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb101_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:50;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:50 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:50;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:49.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:49 from nucleotide 13 to nucleotide 306; the nucleotide sequence of the full-length protein coding sequence of clone yb101_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone yb101_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb101_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:50 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:50, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:50 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:50.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:49.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:49, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:49; and

(ab) the nucleotide sequence of the cDNA insert of clone yb101_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:49, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:49; and

(bb) the nucleotide sequence of the cDNA insert of clone yb101_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:49, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:49 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:49, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:49. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:49 from nucleotide 13 to nucleotide 306, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:49 from nucleotide 13 to nucleotide 306, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:49 from nucleotide 13 to nucleotide 306.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino add sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:50;

(b) a fragment of the amino acid sequence of SEQ ID NO:50, the fragment comprising eight contiguous amino acids of SEQ ID NO:50; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb101_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino add sequence of SEQ ID NO:50. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino add sequence of SEQ ID NO:50 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:50, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:50 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:50.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:51;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:51 from nucleotide 284 to nucleotide 706;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb124_(—)1 deposited under accession number ATCC 98864;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb124_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb124_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb124_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:52;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:52 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:52;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:51.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:51 from nucleotide 284 to nucleotide 706; the nucleotide sequence of the full-length protein coding sequence of clone yb124_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone yb124_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb124_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:52 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:52, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:52 having biological activity, the fragment comprising the amino acid sequence from amino acid 65 to amino acid 74 of SEQ ID NO:52.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:51.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:51, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:51; and

(ab) the nucleotide sequence of the cDNA insert of clone yb124_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:51, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:51; and

(bb) the nucleotide sequence of the cDNA insert of clone yb124_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:51, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:51 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:51, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:51. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:51 from nucleotide 284 to nucleotide 706, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:51 from nucleotide 284 to nucleotide 706, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:51 from nucleotide 284 to nucleotide 706.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:52;

(b) a fragment of the amino acid sequence of SEQ ID NO:52, the fragment comprising eight contiguous amino acids of SEQ ID NO:52; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb124_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:52. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:52 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:52, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:52 having biological activity, the fragment comprising the amino acid sequence from amino acid 65 to amino acid 74 of SEQ ID NO:52.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:53;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:53 from nucleotide 1106 to nucleotide 1447;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:53 from nucleotide 1187 to nucleotide 1447;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb125_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb125_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb125_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb125_(—)1 deposited under accession number ATCC 98864;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:54;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:54 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:54;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:53.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:53 from nucleotide 1106 to nucleotide 1447; the nucleotide sequence of SEQ ID NO:53 from nucleotide 1187 to nucleotide 1447; the nucleotide sequence of the full-length protein coding sequence of clone yb125_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone yb125_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb125_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:54 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:54, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:54 having biological activity, the fragment comprising the amino acid sequence from amino acid 52 to amino acid 61 of SEQ ID NO:54.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:53.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:53, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:53; and

(ab) the nucleotide sequence of the cDNA insert of clone yb125_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:53, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:53; and

(bb) the nucleotide sequence of the cDNA insert of clone yb125_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:53, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:53 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:53, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:53. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:53 from nucleotide 1106 to nucleotide 1447, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:53 from nucleotide 1106 to nucleotide 1447, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:53 from nucleotide 1106 to nucleotide 1447. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:53 from nucleotide 1187 to nucleotide 1447, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:53 from nucleotide 1187 to nucleotide 1447, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:53 from nucleotide 1187 to nucleotide 1447.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:54;

(b) a fragment of the amino acid sequence of SEQ ID NO:54, the fragment comprising eight contiguous amino acids of SEQ ID NO:54; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb125_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:54. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:54 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:54, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:54 having biological activity, the fragment comprising the amino acid sequence from amino acid 52 to amino acid 61 of SEQ ID NO:54.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:55;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:55 from nucleotide 28 to nucleotide 417;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb179_(—)1 deposited under accession number ATCC 98864;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb179_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb179_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb179_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:56;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:56 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:56;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:55.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:55 from nucleotide 28 to nucleotide 417; the nucleotide sequence of the full-length protein coding sequence of clone yb179_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone yb179_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb179_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:56 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:56, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:56 having biological activity, the fragment comprising the amino acid sequence from amino acid 60 to amino acid 69 of SEQ ID NO:56.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:55.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:55, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:55; and

(ab) the nucleotide sequence of the cDNA insert of clone yb179_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:55, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:55; and

(bb) the nucleotide sequence of the cDNA insert of clone yb179_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:55, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:55 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:55, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:55. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:55 from nucleotide 28 to nucleotide 417, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:55 from nucleotide 28 to nucleotide 417, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:55 from nucleotide 28 to nucleotide 417.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:56;

(b) a fragment of the amino acid sequence of SEQ ID NO:56, the fragment comprising eight contiguous amino acids of SEQ ID NO:56; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb179_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:56. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:56 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:56, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:56 having biological activity, the fragment comprising the amino acid sequence from amino acid 60 to amino acid 69 of SEQ ID NO:56.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:57;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:57 from nucleotide 56 to nucleotide 1084;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:57 from nucleotide 107 to nucleotide 1084;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc48_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc48_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc48_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc48_(—)1 deposited under accession number ATCC 98864;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:58;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:58 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:58;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:57.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:57 from nucleotide 56 to nucleotide 1084; the nucleotide sequence of SEQ ID NO:57 from nucleotide 107 to nucleotide 1084; the nucleotide sequence of the full-length protein coding sequence of clone yc48_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone yc48_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc48_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:58 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:58, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:58 having biological activity, the fragment comprising the amino acid sequence from amino acid 166 to amino acid 175 of SEQ ID NO:58.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:57.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:57, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:57; and

(ab) the nucleotide sequence of the cDNA insert of clone yc48_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:57, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:57; and

(bb) the nucleotide sequence of the cDNA insert of done yc48_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(ii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:57, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:57 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:57, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:57. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:57 from nucleotide 56 to nucleotide 1084, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:57 from nucleotide 56 to nucleotide 1084, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:57 from nucleotide 56 to nucleotide 1084. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:57 from nucleotide 107 to nucleotide 1084, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:57 from nucleotide 107 to nucleotide 1084, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ. ID NO:57 from nucleotide 107 to nucleotide 1084.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:58;

(b) a fragment of the amino acid sequence of SEQ ID NO:58, the fragment comprising eight contiguous amino acids of SEQ ID NO:58; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc48_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:58. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:58 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:58, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:58 having biological activity, the fragment comprising the amino acid sequence from amino acid 166 to amino acid 175 of SEQ ID NO:58.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:59;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:59 from nucleotide 373 to nucleotide 660;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:59 from nucleotide 436 to nucleotide 660;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye21_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye21_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye21_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye21_(—)1 deposited under accession number ATCC 98864;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:60;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:60 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:60;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:59.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:59 from nucleotide 373 to nucleotide 660; the nucleotide sequence of SEQ ID NO:59 from nucleotide 436 to nucleotide 660; the nucleotide sequence of the full-length protein coding sequence of clone ye21_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone ye21_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye21_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:60 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:60, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:60 having biological activity, the fragment comprising the amino acid sequence from amino acid 43 to amino acid 52 of SEQ ID NO:60.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:59.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:59, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:59; and

(ab) the nucleotide sequence of the cDNA insert of clone ye21_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:59, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:59; and

(bb) the nucleotide sequence of the cDNA insert of clone ye21_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:59, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:59 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:59, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:59. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:59 from nucleotide 373 to nucleotide 660, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:59 from nucleotide 373 to nucleotide 660, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:59 from nucleotide 373 to nucleotide 660. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:59 from nucleotide 436 to nucleotide 660, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:59 from nucleotide 436 to nucleotide 660, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:59 from nucleotide 436 to nucleotide 660.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:60;

(b) a fragment of the amino acid sequence of SEQ ID NO:60, the fragment comprising eight contiguous amino acids of SEQ ID NO:60; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye21_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:60. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:60 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:60, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:60 having biological activity, the fragment comprising the amino acid sequence from amino acid 43 to amino acid 52 of SEQ ID NO:60.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:61;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:61 from nucleotide 119 to nucleotide 466;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye22_(—)1 deposited under accession number ATCC 98864;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye22_(—)1 deposited under accession number ATCC 98864;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye22_(—)1 deposited under accession number ATCC 98864;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye22_(—)1 deposited under accession number ATCC 98864;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:62;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:62 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:62;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:61.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:61 from nucleotide 119 to nucleotide 466; the nucleotide sequence of the full-length protein coding sequence of clone ye22_(—)1 deposited under accession number ATCC 98864; or the nucleotide sequence of a mature protein coding sequence of clone ye22_(—)1 deposited under accession number ATCC 98864. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye22_(—)1 deposited under accession number ATCC 98864. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:62 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:62, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:62 having biological activity, the fragment comprising the amino acid sequence from amino acid 53 to amino acid 62 of SEQ ID NO:62.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:61.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:61, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:61; and

(ab) the nucleotide sequence of the cDNA insert of clone ye22_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:61, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:61; and

(bb) the nucleotide sequence of the cDNA insert of clone ye22_(—)1 deposited under accession number ATCC 98864;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:61, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:61 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:61, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:61. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:61 from nucleotide 119 to nucleotide 466, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:61 from nucleotide 119 to nucleotide 466, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:61 from nucleotide 119 to nucleotide 466.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:62;

(b) a fragment of the amino acid sequence of SEQ ID NO:62, the fragment comprising eight contiguous amino acids of SEQ ID NO:62; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye22_(—)1 deposited under accession number ATCC 98864;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:62. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:62 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:62, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:62 having biological activity, the fragment comprising the amino acid sequence from amino acid 53 to amino acid 62 of SEQ ID NO:62.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:63;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:63 from nucleotide 1212 to nucleotide 1502;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye39_(—)1 deposited under accession number ATCC 98861;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye39_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye39_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye39_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:64;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:64 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:64;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:63.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:63 from nucleotide 1212 to nucleotide 1502; the nucleotide sequence of the full-length protein coding sequence of clone ye39_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone ye39_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye39_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:64 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:64, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:64 having biological activity, the fragment comprising the amino acid sequence from amino acid 43 to amino acid 52 of SEQ ID NO:64.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:63.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:63, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:63; and

(ab) the nucleotide sequence of the cDNA insert of clone ye39_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:63, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:63; and

(bb) the nucleotide sequence of the cDNA insert of clone ye39_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:63, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:63 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:63, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:63. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:63 from nucleotide 1212 to nucleotide 1502, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:63 from nucleotide 1212 to nucleotide 1502, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:63 from nucleotide 1212 to nucleotide 1502.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:64;

(b) a fragment of the amino acid sequence of SEQ ID NO:64, the fragment comprising eight contiguous amino acids of SEQ ID NO:64; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye39_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:64. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:64 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:64, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:64 having biological activity, the fragment comprising the amino acid sequence from amino acid 43 to amino acid 52 of SEQ ID NO:64.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:65;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:65 from nucleotide 81 to nucleotide 887;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yf9_(—)1 deposited under accession number ATCC 98861;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yf9_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yf9_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yf9_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:66;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:66 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:66;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:65.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:65 from nucleotide 81 to nucleotide 887; the nucleotide sequence of the full-length protein coding sequence of clone yf9_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yf9_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yf9_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:66 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:66, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:66 having biological activity, the fragment comprising the amino acid sequence from amino acid 129 to amino acid 138 of SEQ ID NO:66.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:65.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:65; and

(ab) the nucleotide sequence of the cDNA insert of clone yf9_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:65; and

(bb) the nucleotide sequence of the cDNA insert of clone yf9_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:65, land extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:65 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:65. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:65 from nucleotide 81 to nucleotide 887, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:65 from nucleotide 81 to nucleotide 887, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:65 from nucleotide 81 to nucleotide 887.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:66;

(b) a fragment of the amino acid sequence of SEQ ID NO:66, the fragment comprising eight contiguous amino acids of SEQ ID NO:66; and

(c) the amino acid sequence encoded by the cDNA insert of clone yf9_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:66. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:66 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:66, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:66 having biological activity, the fragment comprising the amino acid sequence from amino acid 129 to amino acid 138 of SEQ ID NO:66.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:67;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:67 from nucleotide 63 to nucleotide 305;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of done yh4_(—)1 deposited under accession number ATCC 98861;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh4_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh4_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh4_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:68;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:68 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO 68;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:67.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:67 from nucleotide 63 to nucleotide 305; the nucleotide sequence of the full-length protein coding sequence of clone yh4_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yh4_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh4_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:68 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:68, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:68 having biological activity, the fragment comprising the amino acid sequence from amino acid 35 to amino acid 44 of SEQ ID NO:68.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:67.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:67, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:67; and

(ab) the nucleotide sequence of the cDNA insert of clone yh4_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:67, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:67; and

(bb) the nucleotide sequence of the cDNA insert of clone yh4_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:67, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:67 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:67, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:67. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:67 from nucleotide 63 to nucleotide 305, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:67 from nucleotide 63 to nucleotide 305, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:67 from nucleotide 63 to nucleotide 305.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:68;

(b) a fragment of the amino acid sequence of SEQ ID NO:68, the fragment comprising eight contiguous amino acids of SEQ ID NO:68; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh4_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:68. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:68 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:68, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:68 having biological activity, the fragment comprising the amino acid sequence from amino acid 35 to amino acid 44 of SEQ ID NO:68.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:69;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:69 from nucleotide 332 to nucleotide 685;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:69 from nucleotide 422 to nucleotide 685;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yi4_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi4_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi4_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi4_(—)1 deposited under accession number ATCC 98861;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:70;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:70 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:70;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:69.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:69 from nucleotide 332 to nucleotide 685; the nucleotide sequence of SEQ ID NO:69 from nucleotide 422 to nucleotide 685; the nucleotide sequence of the full-length protein coding sequence of clone yi4_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yi4_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi4_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:70 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:70, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:70 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:70.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:69.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:69, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:69; and

(ab) the nucleotide sequence of the cDNA insert of done yi4_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:69, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:69; and

(bb) the nucleotide sequence of the cDNA insert of clone yi4_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:69, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:69 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:69, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:69. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:69 from nucleotide 332 to nucleotide 685, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:69 from nucleotide 332 to nucleotide 685, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:69 from nucleotide 332 to nucleotide 685. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:69 from nucleotide 422 to nucleotide 685, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:69 from nucleotide 422 to nucleotide 685, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:69 from nucleotide 422 to nucleotide 685.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:70;

(b) a fragment of the amino acid sequence of SEQ ID NO:70, the fragment comprising eight contiguous amino acids of SEQ ID NO:70; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi4_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:70. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:70 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:70, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:70 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:70.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:71;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:71 from nucleotide 143 to nucleotide 502;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:71 from nucleotide 203 to nucleotide 502;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj3_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj3_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yj3_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj3_(—)1 deposited under accession number ATCC 98861;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:72;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:72 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:72;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:71.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:71 from nucleotide 143 to nucleotide 502; the nucleotide sequence of SEQ ID NO:71 from nucleotide 203 to nucleotide 502; the nucleotide sequence of the full-length protein coding sequence of clone yj3_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yj3_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj3_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:72 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:72, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:72 having biological activity, the fragment comprising the amino acid sequence from amino acid 55 to amino acid 64 of SEQ ID NO:72.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:71.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:71, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:71; and

(ab) the nucleotide sequence of the cDNA insert of clone yj3_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:71, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:71; and

(bb) the nucleotide sequence of the cDNA insert of clone yj3_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:71, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:71 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:71, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:71. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:71 from nucleotide 143 to nucleotide 502, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:71 from nucleotide 143 to nucleotide 502, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:71 from nucleotide 143 to nucleotide 502. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:71 from nucleotide 203 to nucleotide 502, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:71 from nucleotide 203 to nucleotide 502, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:71 from nucleotide 203 to nucleotide 502.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:72;

(b) a fragment of the amino acid sequence of SEQ ID NO:72, the fragment comprising eight contiguous amino acids of SEQ ID NO:72; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj3_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:72. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:72 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:72, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:72 having biological activity, the fragment comprising the amino acid sequence from amino acid 55 to amino acid 64 of SEQ ID NO:72.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:73;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:73 from nucleotide 30 to nucleotide 1004;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:73 from nucleotide 129 to nucleotide 1004;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj7_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj7_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yj7_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj7_(—)1 deposited under accession number ATCC 98861;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:74;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:74 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:74;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:73.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:73 from nucleotide 30 to nucleotide 1004; the nucleotide sequence of SEQ ID NO:73 from nucleotide 129 to nucleotide 1004; the nucleotide sequence of the full-length protein coding sequence of clone yj7_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yj7_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj7_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:74 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:74, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:74 having biological activity, the fragment comprising the amino acid sequence from amino acid 157 to amino acid 166 of SEQ ID NO:74.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:73.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:73, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:73; and

(ab) the nucleotide sequence of the cDNA insert of clone yj7_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:73, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:73; and

(bb) the nucleotide sequence of the cDNA insert of clone yj7_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:73, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:73 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:73, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:73. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:73 from nucleotide 30 to nucleotide 1004, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:73 from nucleotide 30 to nucleotide 1004, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:73 from nucleotide 30 to nucleotide 1004. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:73 from nucleotide 129 to nucleotide 1004, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:73 from nucleotide 129 to nucleotide 1004, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:73 from nucleotide 129 to nucleotide 1004.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:74;

(b) a fragment of the amino acid sequence of SEQ ID NO:74, the fragment comprising eight contiguous amino acids of SEQ ID NO:74; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj7_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:74. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:74 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:74, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:74 having biological activity, the fragment comprising the amino acid sequence from amino acid 157 to amino acid 166 of SEQ ID NO:74.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:75;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:75 from nucleotide 109 to nucleotide 1047;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj10_(—)1 deposited under accession number ATCC 98861;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj10_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yj10_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj10_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:76;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:76 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:76;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:75.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:75 from nucleotide 109 to nucleotide 1047; the nucleotide sequence of the full-length protein coding sequence of done yj10_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yj10_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj10_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:76 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:76, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:76 having biological activity, the fragment comprising the amino acid sequence from amino acid 151 to amino acid 160 of SEQ ID NO:76.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:75.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:75, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:75; and

(ab) the nucleotide sequence of the cDNA insert of clone yj10_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:75, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:75; and

(bb) the nucleotide sequence of the cDNA insert of clone yj10_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:75, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:75 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:75, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:75. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:75 from nucleotide 109 to nucleotide 1047, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:75 from nucleotide 109 to nucleotide 1047, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:75 from nucleotide 109 to nucleotide 1047.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:76;

(b) a fragment of the amino acid sequence of SEQ ID NO:76, the fragment comprising eight contiguous amino acids of SEQ ID NO:76; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj10_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:76. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:76 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:76, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:76 having biological activity, the fragment comprising the amino acid sequence from amino acid 151 to amino acid 160 of SEQ ID NO:76.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:77;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:77 from nucleotide 42 to nucleotide 1196;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:77 from nucleotide 558 to nucleotide 1196;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj28_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj28_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yj28_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj28_(—)1 deposited under accession number ATCC 98861;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:78;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:78 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:78;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:77.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:77 from nucleotide 42 to nucleotide 1196; the nucleotide sequence of SEQ ID NO:77 from nucleotide 558 to nucleotide 1196; the nucleotide sequence of the full-length protein coding sequence of clone yj28_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yj28_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj28_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:78 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:78, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:78 having biological activity, the fragment comprising the amino acid sequence from amino acid 187 to amino acid 196 of SEQ ID NO:78.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:77.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:77, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:77; and

(ab) the nucleotide sequence of the cDNA insert of clone yj28_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:77, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:77; and

(bb) the nucleotide sequence of the cDNA insert of clone yj28_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:77, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:77 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:77, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:77. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:77 from nucleotide 42 to nucleotide 1196, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:77 from nucleotide 42 to nucleotide 1196, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:77 from nucleotide 42 to nucleotide 1196. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:77 from nucleotide 558 to nucleotide 1196, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:77 from nucleotide 558 to nucleotide 1196, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:77 from nucleotide 558 to nucleotide 1196.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:78;

(b) a fragment of the amino acid sequence of SEQ ID NO:78, the fragment comprising eight contiguous amino acids of SEQ ID NO:78; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj28_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:78. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:78 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:78, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:78 having biological activity, the fragment comprising the amino acid sequence from amino acid 187 to amino acid 196 of SEQ ID NO:78.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:79;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:79 from nucleotide 29 to nucleotide 1156;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:79 from nucleotide 995 to nucleotide 1156;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj29_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj29_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of done yj29_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj29_(—)1 deposited under accession number ATCC 98861;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:80;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:80 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:80;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:79.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:79 from nucleotide 29 to nucleotide 1156; the nucleotide sequence of SEQ ID NO:79 from nucleotide 995 to nucleotide 1156; the nucleotide sequence of the full-length protein coding sequence of clone yj29_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yj29_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj29_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:80 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:80, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:80 having biological activity, the fragment comprising the amino acid sequence from amino acid 183 to amino acid 192 of SEQ ID NO:80.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:79.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:79, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:79; and

(ab) the nucleotide sequence of the cDNA insert of clone yj29_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:79, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:79; and

(bb) the nucleotide sequence of the cDNA insert of clone yj29_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:79, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:79 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:79, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:79. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:79 from nucleotide 29 to nucleotide 1156, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:79 from nucleotide 29 to nucleotide 1156, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:79_(—)1 from nucleotide 29 to nucleotide 1156. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:79 from nucleotide 995 to nucleotide 1156, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:79 from nucleotide 995 to nucleotide 1156, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:79 from nucleotide 995 to nucleotide 1156.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:80;

(b) a fragment of the amino acid sequence of SEQ ID NO:80, the fragment comprising eight contiguous amino acids of SEQ ID NO:80; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj29_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:80. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:80 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:80, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:80 having biological activity, the fragment comprising the amino acid sequence from amino acid 183 to amino acid 192 of SEQ ID NO:80.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:81;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:81 from nucleotide 93 to nucleotide 398;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:81 from nucleotide 321 to nucleotide 398;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj32_(—)1 deposited under accession number ATCC 98861;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj32_(—)1 deposited under accession number ATCC 98861;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yj32_(—)1 deposited under accession number ATCC 98861;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj32_(—)1 deposited under accession number ATCC 98861;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:82;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:82 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:82;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:81.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:81 from nucleotide 93 to nucleotide 398; the nucleotide sequence of SEQ ID NO:81 from nucleotide 321 to nucleotide 398; the nucleotide sequence of the full-length protein coding sequence of clone yj32_(—)1 deposited under accession number ATCC 98861; or the nucleotide sequence of a mature protein coding sequence of clone yj32_(—)1 deposited under accession number ATCC 98861. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj32_(—)1 deposited under accession number ATCC 98861. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:82 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:82, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:82 having biological activity, the fragment comprising the amino acid sequence from amino acid 46 to amino acid 55 of SEQ ID NO:82.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:81.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:81, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:81; and

(ab) the nucleotide sequence of the cDNA insert of clone yj32_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:81, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:81; and

(bb) the nucleotide sequence of the cDNA insert of clone yj32_(—)1 deposited under accession number ATCC 98861;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:81, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:81 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:81, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:81. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:81 from nucleotide 93 to nucleotide 398, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:81 from nucleotide 93 to nucleotide 398, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:81 from nucleotide 93 to nucleotide 398. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:81 from nucleotide 321 to nucleotide 398, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:81 from nucleotide 321 to nucleotide 398, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:81 from nucleotide 321 to nucleotide 398.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:82;

(b) a fragment of the amino acid sequence of SEQ ID NO:82, the fragment comprising eight contiguous amino acids of SEQ ID NO:82; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj32_(—)1 deposited under accession number ATCC 98861;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:82. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:82 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:82, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:82 having biological activity, the fragment comprising the amino acid sequence from amino acid 46 to amino acid 55 of SEQ ID NO:82.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:83;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:83 from nucleotide 167 to nucleotide 1264;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:83 from nucleotide 233 to nucleotide 1264;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb186_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb186_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb186_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb186_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:84;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:84 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:84;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:83.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:83 from nucleotide 167 to nucleotide 1264; the nucleotide sequence of SEQ ID NO:83 from nucleotide 233 to nucleotide 1264; the nucleotide sequence of the full-length protein coding sequence of clone yb186_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yb186_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb186_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:84 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:84, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:84 having biological activity, the fragment comprising the amino acid sequence from amino acid 178 to amino acid 187 of SEQ ID NO:84.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:83.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:83, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:83; and

(ab) the nucleotide sequence of the cDNA insert of clone yb186_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:83, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:83; and

(bb) the nucleotide sequence of the cDNA insert of clone yb186_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:83, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:83 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:83, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:83. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:83 from nucleotide 167 to nucleotide 1264, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:83 from nucleotide 167 to nucleotide 1264, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:83 from nucleotide 167 to nucleotide 1264. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:83 from nucleotide 233 to nucleotide 1264, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:83 from nucleotide 233 to nucleotide 1264, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:83 from nucleotide 233 to nucleotide 1264.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:84;

(b) a fragment of the amino acid sequence of SEQ ID NO:84, the fragment comprising eight contiguous amino acids of SEQ ID NO:84; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb186_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:84. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:84 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:84, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:84 having biological activity, the fragment comprising the amino acid sequence from amino acid 178 to amino acid 187 of SEQ ID NO:84.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:85;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:85 from nucleotide 832 to nucleotide 1416;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb226_(—)1 deposited under accession number ATCC 98872;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb226_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb226_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb226_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:86;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:86 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:86;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:85.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:85 from nucleotide 832 to nucleotide 1416; the nucleotide sequence of the full-length protein coding sequence of clone yb226_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yb226_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb226_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:86 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:86, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:86 having biological activity, the fragment comprising the amino acid sequence from amino acid 92 to amino acid 101 of SEQ ID NO:86.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:85.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:85, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:85; and

(ab) the nucleotide sequence of the cDNA insert of clone yb226_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:85, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:85; and

(bb) the nucleotide sequence of the cDNA insert of clone yb226_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:85, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:85 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:85, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:85. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:85 from nucleotide 832 to nucleotide 1416, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:85 from nucleotide 832 to nucleotide 1416, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:85 from nucleotide 832 to nucleotide 1416.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:86;

(b) a fragment of the amino acid sequence of SEQ ID NO:86, the fragment comprising eight contiguous amino acids of SEQ ID NO:86; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb226_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:86. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:86 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:86, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:86 having biological activity, the fragment comprising the amino acid sequence from amino acid 92 to amino acid 101 of SEQ ID NO:86.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:87;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:87 from nucleotide 155 to nucleotide 745;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd50_(—)1 deposited under accession number ATCC 98872;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd50_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd50_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd50_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:88;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:88 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:88;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:87.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:87 from nucleotide 155 to nucleotide 745; the nucleotide sequence of the full-length protein coding sequence of clone yd50_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yd50_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd50_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:88 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:88, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:88 having biological activity, the fragment comprising the amino acid sequence from amino acid 93 to amino acid 102 of SEQ ID NO:88.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:87.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:87, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:87; and

(ab) the nucleotide sequence of the cDNA insert of clone yd50_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:87, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:87; and

(bb) the nucleotide sequence of the cDNA insert of done yd50_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:87, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:87 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:87, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:87. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:87 from nucleotide 155 to nucleotide 745, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:87 from nucleotide 155 to nucleotide 745, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:87 from nucleotide 155 to nucleotide 745.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:88;

(b) a fragment of the amino acid sequence of SEQ ID NO:88, the fragment comprising eight contiguous amino acids of SEQ ID NO:88; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd50_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:88. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:88 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:88, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:88 having biological activity, the fragment comprising the amino acid sequence from amino acid 93 to amino acid 102 of SEQ ID NO:88.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:89;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:89 from nucleotide 42 to nucleotide 317;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:89 from nucleotide 111 to nucleotide 317;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd51_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd51_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd51_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd51_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:90;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:90 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:90;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:89.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:89 from nucleotide 42 to nucleotide 317; the nucleotide sequence of SEQ ID NO:89 from nucleotide 111 to nucleotide 317; the nucleotide sequence of the full-length protein coding sequence of clone yd51_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yd51_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd51_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:90 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:90, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:90 having biological activity, the fragment comprising the amino acid sequence from amino acid 41 to amino acid 50 of SEQ ID NO:90.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:89.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:89, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:89; and

(ab) the nucleotide sequence of the cDNA insert of clone yd51_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:89, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:89; and

(bb) the nucleotide sequence of the cDNA insert of clone yd51_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:89, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:89 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:89, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:89. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:89 from nucleotide 42 to nucleotide 317, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:89 from nucleotide 42 to nucleotide 317, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:89 from nucleotide 42 to nucleotide 317. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:89 from nucleotide 111 to nucleotide 317, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:89 from nucleotide 111 to nucleotide 317, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:89 from nucleotide 111 to nucleotide 317.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:90;

(b) a fragment of the amino acid sequence of SEQ ID NO:90; the fragment comprising eight contiguous amino acids of SEQ ID NO:90; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd51_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:90. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:90 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:90, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:90 having biological activity, the fragment comprising the amino acid sequence from amino acid 41 to amino acid 50 of SEQ ID NO:90.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:91;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:91 from nucleotide 7 to nucleotide 603;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:91 from nucleotide 244 to nucleotide 603;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd73_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd73_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd73_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd73_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:92;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:92 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:92;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:91.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:91 from nucleotide 7 to nucleotide 603; the nucleotide sequence of SEQ ID NO:91 from nucleotide 244 to nucleotide 603; the nucleotide sequence of the full-length protein coding sequence of clone yd73_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yd73_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd73_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:92 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:92, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:92 having biological activity, the fragment comprising the amino acid sequence from amino acid 94 to amino acid 103 of SEQ ID NO:92.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:91.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:91, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:91; and

(ab) the nucleotide sequence of the cDNA insert of clone yd73_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:91, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:91; and

(bb) the nucleotide sequence of the cDNA insert of clone yd73_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:91, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:91 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:91, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:91. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:91 from nucleotide 7 to nucleotide 603, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:91 from nucleotide 7 to nucleotide 603, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:91 from nucleotide 7 to nucleotide 603. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:91 from nucleotide 244 to nucleotide 603, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:91 from nucleotide 244 to nucleotide 603, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:91 from nucleotide 244 to nucleotide 603.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:92;

(b) a fragment of the amino acid sequence of SEQ ID NO:92, the fragment comprising eight contiguous amino acids of SEQ ID NO:92; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd73_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:92. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:92 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:92, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:92 having biological activity, the fragment comprising the amino acid sequence from amino acid 94 to amino acid 103 of SEQ ID NO:92.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:93;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:93 from nucleotide 367 to nucleotide 747;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:93 from nucleotide 667 to nucleotide 747;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye43_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye43_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye43_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye43_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:94;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:94 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:94;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:93.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:93 from nucleotide 367 to nucleotide 747; the nucleotide sequence of SEQ ID NO:93 from nucleotide 667 to nucleotide 747; the nucleotide sequence of the full-length protein coding sequence of clone ye43_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone ye43_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye43_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:94 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:94, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:94 having biological activity, the fragment comprising the amino acid sequence from amino acid 58 to amino acid 67 of SEQ ID NO:94.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:93.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:93, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:93; and

(ab) the nucleotide sequence of the cDNA insert of clone ye43_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:93, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:93; and

(bb) the nucleotide sequence of the cDNA insert of clone ye43_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:93, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:93 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:93, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:93. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:93 from nucleotide 367 to nucleotide 747, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:93 from nucleotide 367 to nucleotide 747, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:93 from nucleotide 367 to nucleotide 747. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:93 from nucleotide 667 to nucleotide 747, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:93 from nucleotide 667 to nucleotide 747, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:93 from nucleotide 667 to nucleotide 747.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:94;

(b) a fragment of the amino acid sequence of SEQ ID NO:94, the fragment comprising eight contiguous amino acids of SEQ ID NO:94; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye43_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:94. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:94 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:94, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:94 having biological activity, the fragment comprising the amino acid sequence from amino acid 58 to amino acid 67 of SEQ ID NO:94.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:95;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:95 from nucleotide 632 to nucleotide 1492;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:95 from nucleotide 1460 to nucleotide 1492;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh71_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh71_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh71_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh71_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:96;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:96 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:96;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:95.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:95 from nucleotide 632 to nucleotide 1492; the nucleotide sequence of SEQ ID NO:95 from nucleotide 1460 to nucleotide 1492; the nucleotide sequence of the full-length protein coding sequence of clone yh71_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yh71_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh71_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:96 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:96, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:96 having biological activity, the fragment comprising the amino acid sequence from amino acid 138 to amino acid 147 of SEQ ID NO:96.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:95.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:95, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:95; and

(ab) the nucleotide sequence of the cDNA insert of clone yh71_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:95, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:95; and

(bb) the nucleotide sequence of the cDNA insert of clone yh71_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:95, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:95 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:95, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:95. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:95 from nucleotide 632 to nucleotide 1492, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:95 from nucleotide 632 to nucleotide 1492, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:95 from nucleotide 632 to nucleotide 1492. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:95 from nucleotide 1460 to nucleotide 1492, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:95 from nucleotide 1460 to nucleotide 1492, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:95 from nucleotide 1460 to nucleotide 1492.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:96;

(b) a fragment of the amino acid sequence of SEQ ID NO:96, the fragment comprising eight contiguous amino acids of SEQ ID NO:96; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh71_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:96. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:96 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:96, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:96 having biological activity, the fragment comprising the amino acid sequence from amino acid 138 to amino acid 147 of SEQ ID NO:96.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:97;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:97 from nucleotide 349 to nucleotide 771;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:97 from nucleotide 490 to nucleotide 771;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh100_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh100_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh100_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh100_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:98;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:98 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:98;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:97.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:97 from nucleotide 349 to nucleotide 771; the nucleotide sequence of SEQ ID NO:97 from nucleotide 490 to nucleotide 771; the nucleotide sequence of the full-length protein coding sequence of clone yh100_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yh100_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh100_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:98 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:98, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:98 having biological activity, the fragment comprising the amino acid sequence from amino acid 65 to amino acid 74 of SEQ ID NO:98.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:97.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:97, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:97; and

(ab) the nucleotide sequence of the cDNA insert of clone yh100_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:97, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:97; and

(bb) the nucleotide sequence of the cDNA insert of clone yh100_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:97, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:97 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:97, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:97. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:97 from nucleotide 349 to nucleotide 771, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:97 from nucleotide 349 to nucleotide 771, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:97 from nucleotide 349 to nucleotide 771. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:97 from nucleotide 490 to nucleotide 771, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:97 from nucleotide 490 to nucleotide 771, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:97 from nucleotide 490 to nucleotide 771.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:98;

(b) a fragment of the amino acid sequence of SEQ ID NO:98, the fragment comprising eight contiguous amino acids of SEQ ID NO:98; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh100_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:98. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:98 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:98, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:98 having biological activity, the fragment comprising the amino acid sequence from amino acid 65 to amino acid 74 of SEQ ID NO:98.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:99;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:99 from nucleotide 165 to nucleotide 416;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:99 from nucleotide 261 to nucleotide 416;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yi3_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi3_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi3_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi3_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:100;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:100 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:100;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:99.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:99 from nucleotide 165 to nucleotide 416; the nucleotide sequence of SEQ ID NO:99 from nucleotide 261 to nucleotide 416; the nucleotide sequence of the full-length protein coding sequence of clone yi3_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yi3_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi3_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:100 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:100, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:100 having biological activity, the fragment comprising the amino acid sequence from amino acid 37 to amino acid 46 of SEQ ID NO:100.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:99.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:99, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:99; and

(ab) the nucleotide sequence of the cDNA insert of clone yi3_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:99, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:99; and

(bb) the nucleotide sequence of the cDNA insert of clone yi3_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:99, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:99 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:99, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:99. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:99 from nucleotide 165 to nucleotide 416, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:99 from nucleotide 165 to nucleotide 416, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:99 from nucleotide 165 to nucleotide 416. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:99 from nucleotide 261 to nucleotide 416, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:99 from nucleotide 261 to nucleotide 416, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:99 from nucleotide 261 to nucleotide 416.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:100;

(b) a fragment of the amino acid sequence of SEQ ID NO:100, the fragment comprising eight contiguous amino acids of SEQ ID NO:100; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi3_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:100. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:100 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:100, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:100 having biological activity, the fragment comprising the amino acid sequence from amino acid 37 to amino acid 46 of SEQ ID NO:100.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:101;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:101 from nucleotide 141 to nucleotide 995;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:101 from nucleotide 213 to nucleotide 995;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yj23_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yj23_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yj23_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yj23_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:102;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:102 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:102;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:101.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:101 from nucleotide 141 to nucleotide 995; the nucleotide sequence of SEQ ID NO:101 from nucleotide 213 to nucleotide 995; the nucleotide sequence of the full-length protein coding sequence of clone yj23_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yj23_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yj23_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:102 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:102, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:102 having biological activity, the fragment comprising the amino acid sequence from amino acid 137 to amino acid 146 of SEQ ID NO:102.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:101.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:101, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:101; and

(ab) the nucleotide sequence of the cDNA insert of clone yj23_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:101, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:101; and

(bb) the nucleotide sequence of the cDNA insert of clone yj23_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:101, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:101 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:101, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:101. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:101 from nucleotide 141 to nucleotide 995, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:101 from nucleotide 141 to nucleotide 995, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:101 from nucleotide 141 to nucleotide 995. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:101 from nucleotide 213 to nucleotide 995, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:101 from nucleotide 213 to nucleotide 995, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:101 from nucleotide 213 to nucleotide 995.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:102;

(b) a fragment of the amino acid sequence of SEQ ID NO:102, the fragment comprising eight contiguous amino acids of SEQ ID NO:102; and

(c) the amino acid sequence encoded by the cDNA insert of clone yj23_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:102. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:102 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:102, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:102 having biological activity, the fragment comprising the amino acid sequence from amino acid 137 to amino acid 146 of SEQ ID NO:102.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:103;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:103 from nucleotide 13 to nucleotide 747;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:103 from nucleotide 67 to nucleotide 747;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yl9_(—)1 deposited under accession number ATCC 98872;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yl9_(—)1 deposited under accession number ATCC 98872;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yl9_(—)1 deposited under accession number ATCC 98872;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yl9_(—)1 deposited under accession number ATCC 98872;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:104;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:104 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:104;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:103.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:103 from nucleotide 13 to nucleotide 747; the nucleotide sequence of SEQ ID NO:103 from nucleotide 67 to nucleotide 747; the nucleotide sequence of the full-length protein coding sequence of clone yl9_(—)1 deposited under accession number ATCC 98872; or the nucleotide sequence of a mature protein coding sequence of clone yl9_(—)1 deposited under accession number ATCC 98872. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yl9_(—)1 deposited under accession number ATCC 98872. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:104 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:104, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:104 having biological activity, the fragment comprising the amino acid sequence from amino acid 117 to amino acid 126 of SEQ ID NO:104.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:103.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:103, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:103; and

(ab) the nucleotide sequence of the cDNA insert of clone yl9_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:103, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:103; and

(bb) the nucleotide sequence of the cDNA insert of clone yl9_(—)1 deposited under accession number ATCC 98872;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:103, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:103 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:103, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:103. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:103 from nucleotide 13 to nucleotide 747, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:103 from nucleotide 13 to nucleotide 747, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:103 from nucleotide 13 to nucleotide 747. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:103 from nucleotide 67 to nucleotide 747, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:103 from nucleotide 67 to nucleotide 747, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:103 from nucleotide 67 to nucleotide 747.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:104;

(b) a fragment of the amino acid sequence of SEQ ID NO:104, the fragment comprising eight contiguous amino acids of SEQ ID NO:104; and

(c) the amino acid sequence encoded by the cDNA insert of clone yl9_(—)1 deposited under accession number ATCC 98872;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:104. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:104 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:104, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:104 having biological activity, the fragment comprising the amino acid sequence from amino acid 117 to amino acid 126 of SEQ ID NO:104.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:105;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:105 from nucleotide 375 to nucleotide 728;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya66_(—)1 deposited under accession number ATCC 98887;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya66_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya66_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya66_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:106;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:106 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:106;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:105.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:105 from nucleotide 375 to nucleotide 728; the nucleotide sequence of the full-length protein coding sequence of clone ya66_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone ya66_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya66_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:106 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:106, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:106 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:106.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:105.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:105, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:105; and

(ab) the nucleotide sequence of the cDNA insert of clone ya66_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:105, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:105; and

(bb) the nucleotide sequence of the cDNA insert of clone ya66_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:105, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:105 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:105, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:105. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:105 from nucleotide 375 to nucleotide 728, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:105 from nucleotide 375 to nucleotide 728, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:105 from nucleotide 375 to nucleotide 728.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:106;

(b) a fragment of the amino acid sequence of SEQ ID NO:106, the fragment comprising eight contiguous amino acids of SEQ ID NO:106; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya66_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:106. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:106 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:106, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:106 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:106.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:107;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:107 from nucleotide 131 to nucleotide 457;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb187_(—)1 deposited under accession number ATCC 98887;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb187_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb187_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb187_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:108;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:108 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:108;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:107.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:107 from nucleotide 131 to nucleotide 457; the nucleotide sequence of the full-length protein coding sequence of clone yb187_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yb187_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb187_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:108 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:108, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:108 having biological activity, the fragment comprising the amino acid sequence from amino acid 49 to amino acid 58 of SEQ ID NO:108.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:107.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:107, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:107; and

(ab) the nucleotide sequence of the cDNA insert of clone yb187_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:107, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:107; and

(bb) the nucleotide sequence of the cDNA insert of clone yb187_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:107, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:107 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:107, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:107. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:107 from nucleotide 131 to nucleotide 457, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:107 from nucleotide 131 to nucleotide 457, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:107 from nucleotide 131 to nucleotide 457.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:108;

(b) a fragment of the amino acid sequence of SEQ ID NO:108, the fragment comprising eight contiguous amino acids of SEQ ID NO:108; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb187_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:108. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:108 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:108, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:108 having biological activity, the fragment comprising the amino acid sequence from amino acid 49 to amino acid 58 of SEQ ID NO:108.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:109;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:109 from nucleotide 458 to nucleotide 676;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:109 from nucleotide 503 to nucleotide 676;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb219_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb219_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb219_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb219_(—)1 deposited under accession number ATCC 98887;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:110;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:110 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:110;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:109.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:109 from nucleotide 458 to nucleotide 676; the nucleotide sequence of SEQ ID NO:109 from nucleotide 503 to nucleotide 676; the nucleotide sequence of the full-length protein coding sequence of clone yb219_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yb219_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb219_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:110 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:110, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:110 having biological activity, the fragment comprising the amino acid sequence from amino acid 31 to amino acid 40 of SEQ ID NO:110.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:109.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:109, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:109; and

(ab) the nucleotide sequence of the cDNA insert of clone yb219_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:109, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:109; and

(bb) the nucleotide sequence of the cDNA insert of clone yb219_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:109, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:109 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:109, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:109. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:109 from nucleotide 458 to nucleotide 676, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:109 from nucleotide 458 to nucleotide 676, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:109 from nucleotide 458 to nucleotide 676. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:109 from nucleotide 503 to nucleotide 676, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:109 from nucleotide 503 to nucleotide 676, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:109 from nucleotide 503 to nucleotide 676.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:110;

(b) a fragment of the amino acid sequence of SEQ ID NO:110, the fragment comprising eight contiguous amino acids of SEQ ID NO:110; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb219_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:110. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:110 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:110, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:110 having biological activity, the fragment comprising the amino acid sequence from amino acid 31 to amino acid 40 of SEQ ID NO:110.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:111;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:111 from nucleotide 238 to nucleotide 396;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:111 from nucleotide 277 to nucleotide 396;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb228_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb228_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb228_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb228_(—)1 deposited under accession number ATCC 98887;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:112;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:112 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:112;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:111.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:111 from nucleotide 238 to nucleotide 396; the nucleotide sequence of SEQ ID NO:111 from nucleotide 277 to nucleotide 396; the nucleotide sequence of the full-length protein coding sequence of clone yb228_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yb228_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb228_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:112 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:112, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:112 having biological activity, the fragment comprising the amino acid sequence from amino acid 21 to amino acid 30 of SEQ ID NO:112.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:111.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:111, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:111; and

(ab) the nucleotide sequence of the cDNA insert of clone yb228_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:111, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:111; and

(bb) the nucleotide sequence of the cDNA insert of clone yb228_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:111, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:111 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:111, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:111. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:111 from nucleotide 238 to nucleotide 396, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:111 from nucleotide 238 to nucleotide 396, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:111 from nucleotide 238 to nucleotide 396. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:111 from nucleotide 277 to nucleotide 396, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:111 from nucleotide 277 to nucleotide 396, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:111 from nucleotide 277 to nucleotide 396.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:112;

(b) a fragment of the amino acid sequence of SEQ ID NO:112, the fragment comprising eight contiguous amino acids of SEQ ID NO:112; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb228_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:112. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:112 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:112, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:112 having biological activity, the fragment comprising the amino acid sequence from amino acid 21 to amino acid 30 of SEQ ID NO:112.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:113;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:113 from nucleotide 6 to nucleotide 722;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:113 from nucleotide 375 to nucleotide 722;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc27_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc27_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc27_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc27_(—)1 deposited under accession number ATCC 98887;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:114;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:114 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:114;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:113.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:113 from nucleotide 6 to nucleotide 722; the nucleotide sequence of SEQ ID NO:113 from nucleotide 375 to nucleotide 722; the nucleotide sequence of the full-length protein coding sequence of clone yc27_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yc27_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc27_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:114 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:114, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:114 having biological activity, the fragment comprising the amino acid sequence from amino acid 114 to amino acid 123 of SEQ ID NO:114.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:113.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:113, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:113; and

(ab) the nucleotide sequence of the cDNA insert of clone yc27_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:113, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:113; and

(bb) the nucleotide sequence of the cDNA insert of clone yc27_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:113, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:113 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:113, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:113. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:113 from nucleotide 6 to nucleotide. 722, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:113 from nucleotide 6 to nucleotide 722, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:113 from nucleotide 6 to nucleotide 722. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:113 from nucleotide 375 to nucleotide 722, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:113 from nucleotide 375 to nucleotide 722, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:113 from nucleotide 375 to nucleotide 722.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:114;

(b) a fragment of the amino acid sequence of SEQ ID NO:114, the fragment comprising eight contiguous amino acids of SEQ ID NO:114; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc27_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:114. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:114 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:114, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:114 having biological activity, the fragment comprising the amino acid sequence from amino acid 114 to amino acid 123 of SEQ ID NO:114.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:115;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:115 from nucleotide 382 to nucleotide 681;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yc49_(—)1 deposited under accession number ATCC 98887;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yc49_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yc49_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yc49_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:116;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:116 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:116;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:115.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:115 from nucleotide 382 to nucleotide 681; the nucleotide sequence of the full-length protein coding sequence of clone yc49_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yc49_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yc49_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:116 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:116, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:116 having biological activity, the fragment comprising the amino acid sequence from amino acid 45 to amino acid 54 of SEQ ID NO:116.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:115.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:115, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:115; and

(ab) the nucleotide sequence of the cDNA insert of clone yc49_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO: 15, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:115; and

(bb) the nucleotide sequence of the cDNA insert of clone yc49_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:115, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:115 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:115, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:115. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:115 from nucleotide 382 to nucleotide 681, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:115 from nucleotide 382 to nucleotide 681, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:115 from nucleotide 382 to nucleotide 681.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:116;

(b) a fragment of the amino acid sequence of SEQ ID NO:116, the fragment comprising eight contiguous amino acids of SEQ ID NO:116; and

(c) the amino acid sequence encoded by the cDNA insert of clone yc49_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:116. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:116 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:116, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:116 having biological activity, the fragment comprising the amino acid sequence from amino acid 45 to amino acid 54 of SEQ ID NO:116.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:117;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:117 from nucleotide 71 to nucleotide 364;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd40_(—)1 deposited under accession number ATCC 98887;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd40_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd40_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd40_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:118;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:118 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:118;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:117.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:117 from nucleotide 71 to nucleotide 364; the nucleotide sequence of the full-length protein coding sequence of clone yd40_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yd40_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd40_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:118 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:118, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:118 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:118.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:117.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:117, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:117; and

(ab) the nucleotide sequence of the cDNA insert of clone yd40_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:117, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:117; and

(bb) the nucleotide sequence of the cDNA insert of clone yd40_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:117, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:117 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:117, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:117. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:117 from nucleotide 71 to nucleotide 364, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:117 from nucleotide 71 to nucleotide 364, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:117 from nucleotide 71 to nucleotide 364.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:118;

(b) a fragment of the amino acid sequence of SEQ ID NO:118, the fragment comprising eight contiguous amino acids of SEQ ID NO:118; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd40_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:118. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:118 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:118, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:118 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:118.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:119;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:119 from nucleotide 75 to nucleotide 725;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd64_(—)1 deposited under accession number ATCC 98887;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd64_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd64_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd64_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:120;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:120 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:120;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:119.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:119 from nucleotide 75 to nucleotide 725; the nucleotide sequence of the full-length protein coding sequence of clone yd64_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yd64_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd64_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:120 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:120, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:120 having biological activity, the fragment comprising the amino acid sequence from amino acid 103 to amino acid 112 of SEQ ID NO:120.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:119.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:119, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:119; and

(ab) the nucleotide sequence of the cDNA insert of clone yd64_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:119, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:119; and

(bb) the nucleotide sequence of the cDNA insert of clone yd64_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:119, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:119 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:119, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:119. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:119 from nucleotide 75 to nucleotide 725, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:119 from nucleotide 75 to nucleotide 725, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:119 from nucleotide 75 to nucleotide 725.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:120;

(b) a fragment of the amino acid sequence of SEQ ID NO:120, the fragment comprising eight contiguous amino acids of SEQ ID NO:120; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd64_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:120. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:120 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:120, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:120 having biological activity, the fragment comprising the amino acid sequence from amino acid 103 to amino acid 112 of SEQ ID NO:120.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:121;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:121 from nucleotide 256 to nucleotide 780;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:121 from nucleotide 412 to nucleotide 780;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye47_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye47_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye47_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye47_(—)1 deposited under accession number ATCC 98887;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:122;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:122 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:122;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:121.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:121 from nucleotide 256 to nucleotide 780; the nucleotide sequence of SEQ ID NO:121 from nucleotide 412 to nucleotide 780; the nucleotide sequence of the full-length protein coding sequence of clone ye47_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone ye47_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye47_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:122 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:122, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:122 having biological activity, the fragment comprising the amino acid sequence from amino acid 82 to amino acid 91 of SEQ ID NO:122.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:121.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:121, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:121; and

(ab) the nucleotide sequence of the cDNA insert of clone ye47_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:121, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:121; and

(bb) the nucleotide sequence of the cDNA insert of clone ye47_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:121, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:121 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:121, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:121. Also preferably the ;polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:12 from nucleotide 256 to nucleotide 780, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:121 from nucleotide 256 to nucleotide 780, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:121 from nucleotide 256 to nucleotide 780. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:121 from nucleotide 412 to nucleotide 780, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:121 from nucleotide 412 to nucleotide 780, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:121 from nucleotide 412 to nucleotide 780.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:122;

(b) a fragment of the amino acid sequence of SEQ ID NO:122, the fragment comprising eight contiguous amino acids of SEQ ID NO:122; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye47_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:122. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:122 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:122, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:22 having biological activity, the fragment comprising the amino acid sequence from amino acid 82 to amino acid 9 of SEQ ID NO:122.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:123;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:123 from nucleotide 127 to nucleotide 405;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:123 from nucleotide 268 to nucleotide 405;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh50_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh50_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh50_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh50_(—)1 deposited under accession number ATCC 98887;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:124;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:124 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:124;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:123.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:123 from nucleotide 127 to nucleotide 405; the nucleotide sequence of SEQ ID NO:123 from nucleotide 268 to nucleotide 405; the nucleotide sequence of the full-length protein coding sequence of clone yh50_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yh50_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh50_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:124 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:124, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:124 having biological activity, the fragment comprising the amino acid sequence from amino acid 41 to amino acid 50 of SEQ ID NO:124.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:123.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:123, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:123; and

(ab) the nucleotide sequence of the cDNA insert of clone yh50_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:123, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:123; and

(bb) the nucleotide sequence of the cDNA insert of clone yh50_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:123, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:123 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:123, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:123. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:123 from nucleotide 127 to nucleotide 405, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:123 from nucleotide 127 to nucleotide 405, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:123 from nucleotide 127 to nucleotide 405. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:123 from nucleotide 268 to nucleotide 405, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:123 from nucleotide 268 to nucleotide 405, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:123 from nucleotide 268 to nucleotide 405.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:124;

(b) a fragment of the amino acid sequence of SEQ ID NO:124, the fragment comprising eight contiguous amino acids of SEQ ID NO:124; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh50_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:124. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:124 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:124, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:124 having biological activity, the fragment comprising the amino acid sequence from amino acid 41 to amino acid 50 of SEQ ID NO:124.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:125;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:125 from nucleotide 1175 to nucleotide 1480;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh53_(—)1 deposited under accession number ATCC 98887;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh53_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh53_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh53_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:126;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:126 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:126;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:125.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:125 from nucleotide 1175 to nucleotide 1480; the nucleotide sequence of the full-length protein coding sequence of clone yh53_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yh53_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh53_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:126 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:126, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:126 having biological activity, the fragment comprising the amino acid sequence from amino acid 46 to amino acid 55 of SEQ ID NO:126.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:125.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:125, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:125; and

(ab) the nucleotide sequence of the cDNA insert of clone yh53_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:125, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:125; and

(bb) the nucleotide sequence of the cDNA insert of clone yh53_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:125, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:125 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:125, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:125. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:125 from nucleotide 1175 to nucleotide 1480, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:125 from nucleotide 1175 to nucleotide 1480, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:125 from nucleotide 1175 to nucleotide 1480.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:126;

(b) a fragment of the amino acid sequence of SEQ ID NO:126, the fragment comprising eight contiguous amino acids of SEQ ID NO:126; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh53_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:126. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:126 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:126, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:126 having biological activity, the fragment comprising the amino acid sequence from amino acid 46 to amino acid 55 of SEQ ID NO:126.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:127;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:127 from nucleotide 65 to nucleotide 319;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:127 from nucleotide 173 to nucleotide 319;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh98_(—)1 deposited under accession number ATCC 98887;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh98_(—)1 deposited under accession number ATCC 98887;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh98_(—)1 deposited under accession number ATCC 98887;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh98_(—)1 deposited under accession number ATCC 98887;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:128;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:128 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:128;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:127.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:127 from nucleotide 65 to nucleotide 319; the nucleotide sequence of SEQ ID NO:127 from nucleotide 173 to nucleotide 319; the nucleotide sequence of the full-length protein coding sequence of clone yh98_(—)1 deposited under accession number ATCC 98887; or the nucleotide sequence of a mature protein coding sequence of clone yh98_(—)1 deposited under accession number ATCC 98887. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh98_(—)1 deposited under accession number ATCC 98887. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:128 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:128, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:128 having biological activity, the fragment comprising the amino acid sequence from amino acid 37 to amino acid 46 of SEQ ID NO:128.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:127.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:127, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:127; and

(ab) the nucleotide sequence of the cDNA insert of clone yh98_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:127, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:127; and

(bb) the nucleotide sequence of the cDNA insert of clone yh98_(—)1 deposited under accession number ATCC 98887;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:127, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:127 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:127, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:127. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:127 from nucleotide 65 to nucleotide 319, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:127 from nucleotide 65 to nucleotide 319, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:127 from nucleotide 65 to nucleotide 319. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:127 from nucleotide 173 to nucleotide 319, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:127 from nucleotide 173 to nucleotide 319, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:127 from nucleotide 173 to nucleotide 319.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:128;

(b) a fragment of the amino acid sequence of SEQ ID NO:128, the fragment comprising eight contiguous amino acids of SEQ ID NO:128; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh98_(—)1 deposited under accession number ATCC 98887;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:128. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:128 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:128, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:128 having biological activity, the fragment comprising the amino acid sequence from amino acid 37 to amino acid 46 of SEQ ID NO:128.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:129;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:129 from nucleotide 122 to nucleotide 469;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:129 from nucleotide 263 to nucleotide 469;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya69_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya69_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya69_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya69_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:130;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:130 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:130;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:129.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:129 from nucleotide 122 to nucleotide 469; the nucleotide sequence of SEQ ID NO:129 from nucleotide 263 to nucleotide 469; the nucleotide sequence of the full-length protein coding sequence of clone ya69_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone ya69_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya69_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:130 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:130, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:130 having biological activity, the fragment comprising the amino acid sequence from amino acid 53 to amino acid 62 of SEQ ID NO:130.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:129.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:129, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:129; and

(ab) the nucleotide sequence of the cDNA insert of clone ya69_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:129, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:129; and

(bb) the nucleotide sequence of the cDNA insert of clone ya69_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:129, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:129 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:129, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:129. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:129 from nucleotide 122 to nucleotide 469, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:129 from nucleotide 122 to nucleotide 469, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:129 from nucleotide 122 to nucleotide 469. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:129 from nucleotide 263 to nucleotide 469, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:129 from nucleotide 263 to nucleotide 469, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:129 from nucleotide 263 to nucleotide 469.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:130;

(b) a fragment of the amino acid sequence of SEQ ID NO:130, the fragment comprising eight contiguous amino acids of SEQ ID NO:130; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya69_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:130. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:130 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:130, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:130 having biological activity, the fragment comprising the amino acid sequence from amino acid 53 to amino acid 62 of SEQ ID NO:130.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:131;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:131 from nucleotide 36 to nucleotide 554;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:131 from nucleotide 183 to nucleotide 554;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd107_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd107_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd107_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd107_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:132;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:132 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:132;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:131.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:131 from nucleotide 36 to nucleotide 554; the nucleotide sequence of SEQ ID NO:131 from nucleotide 183 to nucleotide 554; the nucleotide sequence of the full-length protein coding sequence of clone yd107_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yd107_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd107_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:132 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:132, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:132 having biological activity, the fragment comprising the amino acid sequence from amino acid 81 to amino acid 90 of SEQ ID NO:132.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:131.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:131, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:131; and

(ab) the nucleotide sequence of the cDNA insert of clone yd107_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:131, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:131; and

(bb) the nucleotide sequence of the cDNA insert of clone yd107_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:131, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:131 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:131, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:131. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:131 from nucleotide 36 to nucleotide 554, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:131 from nucleotide 36 to nucleotide 554, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:131 from nucleotide 36 to nucleotide 554. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:131 from nucleotide 183 to nucleotide 554, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:131 from nucleotide 183 to nucleotide 554, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:131 from nucleotide 183 to nucleotide 554.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:132;

(b) a fragment of the amino acid sequence of SEQ ID NO:132, the fragment comprising eight contiguous amino acids of SEQ ID NO:132; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd107_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:132. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:132 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:132, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:132 having biological activity, the fragment comprising the amino acid sequence from amino acid 81 to amino acid 90 of SEQ ID NO:132.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:133;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:133 from nucleotide 8 to nucleotide 493;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:133 from nucleotide 53 to nucleotide 493;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd145_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd145_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd145_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd145_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:134;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:134 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:134;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:133.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:133 from nucleotide 8 to nucleotide 493; the nucleotide sequence of SEQ ID NO:133 from nucleotide 53 to nucleotide 493; the nucleotide sequence of the full-length protein coding sequence of clone yd145_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yd145_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd145_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:134 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:134, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:134 having biological activity, the fragment comprising the amino acid sequence from amino acid 76 to amino acid 85 of SEQ ID NO:134.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:133.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:133, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:133; and

(ab) the nucleotide sequence of the cDNA insert of clone yd145_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:133, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:133; and

(bb) the nucleotide sequence of the cDNA insert of clone yd145_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:133, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:133 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:133, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:133. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:133 from nucleotide 8 to nucleotide 493, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:133 from nucleotide 8 to nucleotide 493, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:133 from nucleotide 8 to nucleotide 493. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:133 from nucleotide 53 to nucleotide 493, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:133 from nucleotide 53 to nucleotide 493, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:133 from nucleotide 53 to nucleotide 493.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:134;

(b) a fragment of the amino acid sequence of SEQ ID NO:134, the fragment comprising eight contiguous amino acids of SEQ ID NO:134; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd145_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:134. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:134 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:134, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:134 having biological activity, the fragment comprising the amino acid sequence from amino acid 76 to amino acid 85 of SEQ ID NO:134.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:135;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:135 from nucleotide 21 to nucleotide 308;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh24_(—)1 deposited under accession number ATCC 98915;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh24_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh24_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh24_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:136;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:136 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:136;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:135.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:135 from nucleotide 21 to nucleotide 308; the nucleotide sequence of the full-length protein coding sequence of clone yh24_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yh24_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh24_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:136 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:136, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:136 having biological activity, the fragment comprising the amino acid sequence from amino acid 43 to amino acid 52 of SEQ ID NO:136.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:135.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:135, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:135; and

(ab) the nucleotide sequence of the cDNA insert of clone yh24_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:135, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:135; and

(bb) the nucleotide sequence of the cDNA insert of clone yh24_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:135, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:135 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:135, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:135. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:135 from nucleotide 21 to nucleotide 308, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:135 from nucleotide 21 to nucleotide 308, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:135 from nucleotide 21 to nucleotide 308.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:136;

(b) a fragment of the amino acid sequence of SEQ ID NO:136, the fragment comprising eight contiguous amino acids of SEQ ID NO:136; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh24_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:136. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:136 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:136, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:136 having biological activity, the fragment comprising the amino acid sequence from amino acid 43 to amino acid 52 of SEQ ID NO:136.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID. NO:137;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:137 from nucleotide 214 to nucleotide 735;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:137 from nucleotide 634 to nucleotide 735;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yi11_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi11_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi11_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi11_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:138;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:138 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:138;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:137.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:137 from nucleotide 214 to nucleotide 735; the nucleotide sequence of SEQ ID NO:137 from nucleotide 634 to nucleotide 735; the nucleotide sequence of the full-length protein coding sequence of clone yi11_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yi11_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi11_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:138 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:138, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:138 having biological activity, the fragment comprising the amino acid sequence from amino acid 82 to amino acid 91 of SEQ ID NO:138.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:137.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:137, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:137; and

(ab) the nucleotide sequence of the cDNA insert of clone yi11_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:137, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:137; and

(bb) the nucleotide sequence of the cDNA insert of clone yi11_(—)1 deposited under accession number ATCC 98915;

(j) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:137, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:137 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:137, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:137. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:137 from nucleotide 214 to nucleotide 735, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:137 from nucleotide 214 to nucleotide 735, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:137 from nucleotide 214 to nucleotide 735. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:137 from nucleotide 634 to nucleotide 735, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:137 from nucleotide 634 to nucleotide 735, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:137 from nucleotide 634 to nucleotide 735.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:138;

(b) a fragment of the amino acid sequence of SEQ ID NO:138, the fragment comprising eight contiguous amino acids of SEQ ID NO:138; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi11_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:138. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:138 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:138, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:138 having biological activity, the fragment comprising the amino acid sequence from amino acid 82 to amino acid 91 of SEQ ID NO:138.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:139;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:139 from nucleotide 668 to nucleotide 937;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:139 from nucleotide 848 to nucleotide 937;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yi18_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi18_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi18_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi18_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:140;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:140 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:140;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:139.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:139 from nucleotide 668 to nucleotide 937; the nucleotide sequence of SEQ ID NO:139 from nucleotide 848 to nucleotide 937; the nucleotide sequence of the full-length protein coding sequence of clone yi18_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yi18_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi18_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:140 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:140, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:140 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:140.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:139.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:139, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:139; and

(ab) the nucleotide sequence of the cDNA insert of clone yi18_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:139, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:139; and

(bb) the nucleotide sequence of the cDNA insert of clone yi18_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:139, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:139 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:139, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:139. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:139 from nucleotide 668 to nucleotide 937, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:139 from nucleotide 668 to nucleotide 937, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:139 from nucleotide 668 to nucleotide 937. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:139 from nucleotide 848 to nucleotide 937, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:139 from nucleotide 848 to nucleotide 937, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:139 from nucleotide 848 to nucleotide 937.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO: 140;

(b) a fragment of the amino acid sequence of SEQ ID NO:140, the fragment comprising eight contiguous amino acids of SEQ ID NO:140; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi18_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:140. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:140 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:140, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:140 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:140.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:141;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:141 from nucleotide 171 to nucleotide 407;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:141 from nucleotide 258 to nucleotide 407;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk14_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk14_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk14_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk14_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:142;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:142 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:142;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:141.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:141 from nucleotide 171 to nucleotide 407; the nucleotide sequence of SEQ ID NO:141 from nucleotide 258 to nucleotide 407; the nucleotide sequence of the full-length protein coding sequence of clone yk14_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yk14_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk14_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:142 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:142, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:142 having biological activity, the fragment comprising the amino acid sequence from amino acid 34 to amino acid 43 of SEQ ID NO:142.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:141.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:141, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:141; and

(ab) the nucleotide sequence of the cDNA insert of clone yk14_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:141, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:141; and

(bb) the nucleotide sequence of the cDNA insert of clone yk14_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:141, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:141 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:141, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:141. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:141 from nucleotide 171 to nucleotide 407, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:141 from nucleotide 171 to nucleotide 407, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:141 from nucleotide 171 to nucleotide 407. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:141 from nucleotide 258 to nucleotide 407, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:141 from nucleotide 258 to nucleotide 407, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:141 from nucleotide 258 to nucleotide 407.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:142;

(b) a fragment of the amino acid sequence of SEQ ID NO:142, the fragment comprising eight contiguous amino acids of SEQ ID NO:142; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk14_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:142. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:142 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:142, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:142 having biological activity, the fragment comprising the amino acid sequence from amino acid 34 to amino acid 43 of SEQ ID NO:142.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:143;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:143 from nucleotide 164 to nucleotide 457;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk39_(—)1 deposited under accession number ATCC 98915;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk39_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk39_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk39_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:144;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:144 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:144;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:143.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:143 from nucleotide 164 to nucleotide 457; the nucleotide sequence of the full-length protein coding sequence of clone yk39_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yk39_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk39_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:144 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:144, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:144 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:144.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:143.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:143, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:143; and

(ab) the nucleotide sequence of the cDNA insert of clone yk39_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:143, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:143; and

(bb) the nucleotide sequence of the cDNA insert of clone yk39_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:143, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:143 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:143, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:143. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:143 from nucleotide 164 to nucleotide 457, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:143 from nucleotide 164 to nucleotide 457, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:143 from nucleotide 164 to nucleotide 457.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:144;

(b) a fragment of the amino acid sequence of SEQ ID NO:144, the fragment comprising eight contiguous amino acids of SEQ ID NO:144; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk39_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:144. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:144 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:144, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:144 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:144.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:145;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:145 from nucleotide 72 to nucleotide 500;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 145 from nucleotide 255 to nucleotide 500;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk91_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk91_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk91_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk91_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:146;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:146 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:146;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:145.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:145 from nucleotide 72 to nucleotide 500; the nucleotide sequence of SEQ ID NO:145 from nucleotide 255 to nucleotide 500; the nucleotide sequence of the full-length protein coding sequence of clone yk91_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yk91_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk91_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:146 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:146, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:146 having biological activity, the fragment comprising the amino acid sequence from amino acid 66 to amino acid 75 of SEQ ID NO:146.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:145.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:145, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:145; and

(ab) the nucleotide sequence of the cDNA insert of clone yk91_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:145, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:145; and

(bb) the nucleotide sequence of the cDNA insert of clone yk91_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:145, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:145 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:145, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:145. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:145 from nucleotide 72 to nucleotide 500, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:145 from nucleotide 72 to nucleotide 500, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:145 from nucleotide 72 to nucleotide 500. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:145 from nucleotide 255 to nucleotide 500, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:145 from nucleotide 255 to nucleotide 500, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:145 from nucleotide 255 to nucleotide 500.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:146;

(b) a fragment of the amino acid sequence of SEQ ID NO:146, the fragment comprising eight contiguous amino acids of SEQ ID NO:146; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk91_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:146. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:146 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:146, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:146 having biological activity, the fragment comprising the amino acid sequence from amino acid 66 to amino acid 75 of SEQ ID NO:146.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:147;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:147 from nucleotide 174 to nucleotide 620;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:147 from nucleotide 240 to nucleotide 620;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk199_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk199_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk199_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk199_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:148;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:148 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:148;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:147.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:147 from nucleotide 174 to nucleotide 620; the nucleotide sequence of SEQ ID NO:147 from nucleotide 240 to nucleotide 620; the nucleotide sequence of the full-length protein coding sequence of clone yk199_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yk199_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of done yk199_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:148 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:148, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:148 having biological activity, the fragment comprising the amino acid sequence from amino acid 69 to amino acid 78 of SEQ ID NO:148.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:147.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:147, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:147; and

(ab) the nucleotide sequence of the cDNA insert of clone yk199_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:147, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:147; and

(bb) the nucleotide sequence of the cDNA insert of clone yk199_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:147, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:147 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:147, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:147. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:147 from nucleotide 174 to nucleotide 620, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:147 from nucleotide 174 to nucleotide 620, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:147 from nucleotide 174 to nucleotide 620. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:147 from nucleotide 240 to nucleotide 620, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:147 from nucleotide 240 to nucleotide 620, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:147 from nucleotide 240 to nucleotide 620.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:148;

(b) a fragment of the amino acid sequence of SEQ ID NO:148, the fragment comprising eight contiguous amino acids of SEQ ID NO:148; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk199_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:148. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:148 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:148, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:148 having biological activity, the fragment comprising the amino acid sequence from amino acid 69 to amino acid 78 of SEQ ID NO:148.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:149;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:149 from nucleotide 325 to nucleotide 984;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:149 from nucleotide 973 to nucleotide 984;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yl4_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yl4_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yl4_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yl4_(—)1 deposited under accession number ATCC 98915;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:150;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:150 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:150;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:149.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:149 from nucleotide 325 to nucleotide 984; the nucleotide sequence of SEQ ID NO:149 from nucleotide 973 to nucleotide 984; the nucleotide sequence of the full-length protein coding sequence of clone yl4_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yl4_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yl4_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:150 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:150, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:150 having biological activity, the fragment comprising the amino acid sequence from amino acid 105 to amino acid 114 of SEQ ID NO:150.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:149.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:149, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:149; and

(ab) the nucleotide sequence of the cDNA insert of clone yl4_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:149, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:149; and

(bb) the nucleotide sequence of the cDNA insert of clone yl4_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:149, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:149 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:149, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:149. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:149 from nucleotide 325 to nucleotide 984, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:149 from nucleotide 325 to nucleotide 984, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:149 from nucleotide 325 to nucleotide 984. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:149 from nucleotide 973 to nucleotide 984, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:149 from nucleotide 973 to nucleotide 984, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO: 149 from nucleotide 973 to nucleotide 984.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:150;

(b) a fragment of the amino acid sequence of SEQ ID NO:150, the fragment comprising eight contiguous amino acids of SEQ ID NO:150; and

(c) the amino acid sequence encoded by the cDNA insert of clone yl4_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:150. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:150 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:150, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:150 having biological activity, the fragment comprising the amino acid sequence from amino acid 105 to amino acid 114 of SEQ ID NO:150.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:151;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:151 from nucleotide 119 to nucleotide 415;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yl14_(—)1 deposited under accession number ATCC 98915;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yl14_(—)1 deposited under accession number ATCC 98915;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yl14_(—)1 deposited under accession number ATCC 98915;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yl14_(—)1 deposited under accession number ATCC 98915;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:152;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:152 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:152;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:151.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:151 from nucleotide 119 to nucleotide 415; the nucleotide sequence of the full-length protein coding sequence of clone yl14_(—)1 deposited under accession number ATCC 98915; or the nucleotide sequence of a mature protein coding sequence of clone yl14_(—)1 deposited under accession number ATCC 98915. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yl14_(—)1 deposited under accession number ATCC 98915. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:152 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:152, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:152 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:152.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:151.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:151, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:151; and

(ab) the nucleotide sequence of the cDNA insert of clone yl14_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:151, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:151; and

(bb) the nucleotide sequence of the cDNA insert of clone yl14_(—)1 deposited under accession number ATCC 98915;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:151, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:151 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:151, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:151. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:151 from nucleotide 119 to nucleotide 415, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:151 from nucleotide 119 to nucleotide 415, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:151 from nucleotide 119 to nucleotide 415.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:152;

(b) a fragment of the amino acid sequence of SEQ ID NO:152, the fragment comprising eight contiguous amino acids of SEQ ID NO:152; and

(c) the amino acid sequence encoded by the cDNA insert of clone yl14_(—)1 deposited under accession number ATCC 98915;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:152. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:152 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:152, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:152 having biological activity, the fragment comprising the amino acid sequence from amino acid 44 to amino acid 53 of SEQ ID NO:152.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:153;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:153 from nucleotide 96 to nucleotide 377;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:153 from nucleotide 225 to nucleotide 377;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ya80_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ya80_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ya80_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ya80_(—)1 deposited under accession number ATCC 98925;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:154;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:154 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:154;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:153.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:153 from nucleotide 96 to nucleotide 377; the nucleotide sequence of SEQ ID NO:153 from nucleotide 225 to nucleotide 377; the nucleotide sequence of the full-length protein coding sequence of clone ya80_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone ya80_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ya80_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:154 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:154, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:154 having biological activity, the fragment comprising the amino acid sequence from amino acid 42 to amino acid 51 of SEQ ID NO:154.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:153.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:153, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:153; and

(ab) the nucleotide sequence of the cDNA insert of done ya80_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:153, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:153; and

(bb) the nucleotide sequence of the cDNA insert of clone ya80_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:153, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:153 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:153, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:153. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:153 from nucleotide 96 to nucleotide 377, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:153 from nucleotide 96 to nucleotide 377, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:153 from nucleotide 96 to nucleotide 377. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:153 from nucleotide 225 to nucleotide 377, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:153 from nucleotide 225 to nucleotide 377, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:153 from nucleotide 225 to nucleotide 377.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:154;

(b) a fragment of the amino acid sequence of SEQ ID NO:154, the fragment comprising eight contiguous amino acids of SEQ ID NO:154; and

(c) the amino acid sequence encoded by the cDNA insert of clone ya80_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:154. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:154 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:154, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:154 having biological activity, the fragment comprising the amino acid sequence from amino acid 42 to amino acid 51 of SEQ ID NO:154.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:155;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:155 from nucleotide 118 to nucleotide 681;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:155 from nucleotide 622 to nucleotide 681;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd61_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd61_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd61_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd61_(—)1 deposited under accession number ATCC 98925;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:156;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:156 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:156;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:155.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:155 from nucleotide 118 to nucleotide 681; the nucleotide sequence of SEQ ID NO:155 from nucleotide 622 to nucleotide 681; the nucleotide sequence of the full-length protein coding sequence of clone yd61_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd61_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd61_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:156 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:156, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:156 having biological activity, the fragment comprising the amino acid sequence from amino acid 89 to amino acid 98 of SEQ ID NO:156.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:155.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:155, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:155; and

(ab) the nucleotide sequence of the cDNA insert of clone yd61_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:155, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:155; and

(bb) the nucleotide sequence of the cDNA insert of clone yd61_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:155, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:155 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:155, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:155. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:155 from nucleotide 118 to nucleotide 681, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:155 from nucleotide 118 to nucleotide 681, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:155 from nucleotide 118 to nucleotide 681. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:155 from nucleotide 622 to nucleotide 681, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:155 from nucleotide 622 to nucleotide 681, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:155 from nucleotide 622 to nucleotide 681.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:156;

(b) a fragment of the amino acid sequence of SEQ ID NO:156, the fragment comprising eight contiguous amino acids of SEQ ID NO:156; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd61_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:156. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:156 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:156, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:156 having biological activity, the fragment comprising the amino acid sequence from amino acid 89 to amino acid 98 of SEQ ID NO:156.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:157;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:157 from nucleotide 261 to nucleotide 614;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd88_(—)1 deposited under accession number ATCC 98925;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd88_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd88_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd88_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:158;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:158 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:158;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:157.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:157 from nucleotide 261 to nucleotide 614; the nucleotide sequence of the full-length protein coding sequence of clone yd88_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd88_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd88_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:158 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:158, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:158 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:158.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:157.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:157, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:157; and

(ab) the nucleotide sequence of the cDNA insert of clone yd88_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:157, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:157; and

(bb) the nucleotide sequence of the cDNA insert of clone yd88_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:157, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:157 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:157, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:157. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:157 from nucleotide 261 to nucleotide 614, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:157 from nucleotide 261 to nucleotide 614, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:157 from nucleotide 261 to nucleotide 614.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:158;

(b) a fragment of the amino acid sequence of SEQ ID NO:158, the fragment comprising eight contiguous amino acids of SEQ ID NO:158; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd88_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:158. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:158 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:158, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:158 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:158.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:159;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:159 from nucleotide 26 to nucleotide 475;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd109_(—)1 deposited under accession number ATCC 98925;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd109_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd109_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd109_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:160;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:160 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:160;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:159.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:159 from nucleotide 26 to nucleotide 475; the nucleotide sequence of the full-length protein coding sequence of clone yd109_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd109_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd109_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:160 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:160, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:160 having biological activity, the fragment comprising the amino acid sequence from amino acid 70 to amino acid 79 of SEQ ID NO:160.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:159.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:159, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:159; and

(ab) the nucleotide sequence of the cDNA insert of clone yd109_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:159, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:159; and

(bb) the nucleotide sequence of the cDNA insert of done yd109_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:159, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:159 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:159, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:159. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:159 from nucleotide 26 to nucleotide 475, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:159 from nucleotide 26 to nucleotide 475, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:159 from nucleotide 26 to nucleotide 475.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:160;

(b) a fragment of the amino acid sequence of SEQ ID NO:160, the fragment comprising eight contiguous amino acids of SEQ ID NO:160; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd109_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:160. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:160 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:160, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:160 having biological activity, the fragment comprising the amino acid sequence from amino acid 70 to amino acid 79 of SEQ ID NO:160.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:161;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:161 from nucleotide 79 to nucleotide 474;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd141_(—)1 deposited under accession number ATCC 98925;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd141_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd141_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd141_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:162;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:162 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:162;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:161.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:161 from nucleotide 79 to nucleotide 474; the nucleotide sequence of the full-length protein coding sequence of clone yd141_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd141_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd141_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:162 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:162, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:162 having biological activity, the fragment comprising the amino acid sequence from amino acid 61 to amino acid 70 of SEQ ID NO:162.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:161.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:161, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:161; and

(ab) the nucleotide sequence of the cDNA insert of done yd141_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:161, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:161; and

(bb) the nucleotide sequence of the cDNA insert of done yd141_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:161, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:161 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:161, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:161. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:161 from nucleotide 79 to nucleotide 474, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:161 from nucleotide 79 to nucleotide 474, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:161 from nucleotide 79 to nucleotide 474.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:162;

(b) a fragment of the amino acid sequence of SEQ ID NO:162, the fragment comprising eight contiguous amino acids of SEQ ID NO:162; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd141_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:162. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:162 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:162, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:162 having biological activity, the fragment comprising the amino acid sequence from amino acid 61 to amino acid 70 of SEQ ID NO:162.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:163;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:163 from nucleotide 45 to nucleotide 347;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:163 from nucleotide 135 to nucleotide 347;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd153_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd153_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd153_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd153_(—)1 deposited under accession number ATCC 98925;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:164;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:164 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:164;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:163.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:163 from nucleotide 45 to nucleotide 347; the nucleotide sequence of SEQ ID NO:163 from nucleotide 135 to nucleotide 347; the nucleotide sequence of the full-length protein coding sequence of clone yd153_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd153_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd153_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:164 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:164, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:164 having biological activity, the fragment comprising the amino acid sequence from amino acid 45 to amino acid 54 of SEQ ID NO:164.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:163.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:163, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:163; and

(ab) the nucleotide sequence of the cDNA insert of clone yd153_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:163, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:163; and

(bb) the nucleotide sequence of the cDNA insert of clone yd153_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:163, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:163 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:163, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:163. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:163 from nucleotide 45 to nucleotide 347, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:163 from nucleotide 45 to nucleotide 347, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:163 from nucleotide 45 to nucleotide 347. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:163 from nucleotide 135 to nucleotide 347, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:163 from nucleotide 135 to nucleotide 347, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:163 from nucleotide 135 to nucleotide 347.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:164;

(b) a fragment of the amino acid sequence of SEQ ID NO:164, the fragment comprising eight contiguous amino acids of SEQ ID NO:164; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd153_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:164. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:164 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:164, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:164 having biological activity, the fragment comprising the amino acid sequence from amino acid 45 to amino acid 54 of SEQ ID NO:164.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:165;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:165 from nucleotide 114 to nucleotide 470;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd165_(—)1 deposited under accession number ATCC 98925;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd165_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd165_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd165_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:166;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:166 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:166;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:165.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:165 from nucleotide 114 to nucleotide 470; the nucleotide sequence of the full-length protein coding sequence of clone yd165_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd165_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd165_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:166 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:166, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:166 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:166.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:165.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:165, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:165; and

(ab) the nucleotide sequence of the cDNA insert of clone yd165_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:165, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:165; and

(bb) the nucleotide sequence of the cDNA insert of clone yd165_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:165, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:165 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:165, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:165. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:165 from nucleotide 114 to nucleotide 470, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:165 from nucleotide 114 to nucleotide 470, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:165 from nucleotide 114 to nucleotide 470.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:166;

(b) a fragment of the amino acid sequence of SEQ ID NO:166, the fragment comprising eight contiguous amino acids of SEQ ID NO:166; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd165_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:166. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:166 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:166, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:166 having biological activity, the fragment comprising the amino acid sequence from amino acid 54 to amino acid 63 of SEQ ID NO:166.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:167;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:167 from nucleotide 82 to nucleotide 663;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:167 from nucleotide 139 to nucleotide 663;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd178_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd178_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd178_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd178_(—)1 deposited under accession number ATCC 98925;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:168;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:168 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:168;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:167.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:167 from nucleotide 82 to nucleotide 663; the nucleotide sequence of SEQ ID NO:167 from nucleotide 139 to nucleotide 663; the nucleotide sequence of the full-length protein coding sequence of clone yd178_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd178_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd178_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:168 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:168, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:168 having biological activity, the fragment comprising the amino acid sequence from amino acid 92 to amino acid 101 of SEQ ID NO:168.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:167.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:167, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:167; and

(ab) the nucleotide sequence of the cDNA insert of clone yd178_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:167, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:167; and

(bb) the nucleotide sequence of the cDNA insert of clone yd178_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:167, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:167 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:167, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:167. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:167 from nucleotide 82 to nucleotide 663, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:167 from nucleotide 82 to nucleotide 663, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:167 from nucleotide 82 to nucleotide 663. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:167 from nucleotide 139 to nucleotide 663, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:167 from nucleotide 139 to nucleotide 663, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:167 from nucleotide 139 to nucleotide 663.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:168;

(b) a fragment of the amino acid sequence of SEQ ID NO:168, the fragment comprising eight contiguous amino acids of SEQ ID NO:168; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd178_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:168. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:168 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:168, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:168 having biological activity, the fragment comprising the amino acid sequence from amino acid 92 to amino acid 101 of SEQ ID NO:168.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:169;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:169 from nucleotide 121 to nucleotide 450;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd191_(—)1 deposited under accession number ATCC 98925;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd191_(—)1 deposited under accession number ATCC 98925;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd191_(—)1 deposited under accession number ATCC 98925;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd191_(—)1 deposited under accession number ATCC 98925;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO: 170;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:170 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:170;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:169.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO: 169 from nucleotide 121 to nucleotide 450; the nucleotide sequence of the full length protein coding sequence of clone yd191_(—)1 deposited under accession number ATCC 98925; or the nucleotide sequence of a mature protein coding sequence of clone yd191_(—)1 deposited under accession number ATCC 98925. In other preferred embodiments, the polynucleotide encodes the full length or a mature protein encoded by the cDNA insert of clone yd191_(—)1 deposited under accession number ATCC 98925. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:170 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:170, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:170 having biological activity, the fragment comprising the amino acid sequence from amino acid 50 to amino acid 59 of SEQ ID NO:170.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:169.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:169, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:169; and

(ab) the nucleotide sequence of the cDNA insert of clone yd191_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:169, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:169; and

(bb) the nucleotide sequence of the cDNA insert of clone yd191_(—)1 deposited under accession number ATCC 98925;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:169, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:169 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:169, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:169. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:169 from nucleotide 121 to nucleotide 450, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:169 from nucleotide 121 to nucleotide 450, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:169 from nucleotide 121 to nucleotide 450.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:170;

(b) a fragment of the amino acid sequence of SEQ ID NO:170, the fragment comprising eight contiguous amino acids of SEQ ID NO:170; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd191_(—)1 deposited under accession number ATCC 98925;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:170. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:170 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:170, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:170 having biological activity, the fragment comprising the amino acid sequence from amino acid 50 to amino acid 59 of SEQ ID NO:170.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:171;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:171 from nucleotide 33 to nucleotide 494;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ye7_(—)1 deposited under accession number ATCC 98924;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ye7_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ye7_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ye7_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:172;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:172 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:172;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:171.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:171 from nucleotide 33 to nucleotide 494; the nucleotide sequence of the full-length protein coding sequence of clone ye7_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone ye7_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ye7_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:172 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:172, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:172 having biological activity, the fragment comprising the amino acid sequence from amino acid 72 to amino acid 81 of SEQ ID NO:172.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:171.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:171, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:171; and

(ab) the nucleotide sequence of the cDNA insert of done ye7_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:171, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:171; and

(bb) the nucleotide sequence of the cDNA insert of clone ye7_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:171, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:171 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:171, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:171. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:171 from nucleotide 33 to nucleotide 494, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:171 from nucleotide 33 to nucleotide 494, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:171 from nucleotide 33 to nucleotide 494.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:172;

(b) a fragment of the amino acid sequence of SEQ ID NO:172, the fragment comprising eight contiguous amino acids of SEQ ID NO:172; and

(c) the amino acid sequence encoded by the cDNA insert of clone ye7_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:172. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:172 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:172, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:172 having biological activity, the fragment comprising the amino acid sequence from amino acid 72 to amino acid 81 of SEQ ID NO:172.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:173;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:173 from nucleotide 1251 to nucleotide 1625;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:173 from nucleotide 1395 to nucleotide 1625;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yf33_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yf33_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yf33_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yf33_(—)1 deposited under accession number ATCC 98924;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:174;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:174 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:174;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:173.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:173 from nucleotide 1251 to nucleotide 1625; the nucleotide sequence of SEQ ID NO:173 from nucleotide 1395 to nucleotide 1625; the nucleotide sequence of the full-length protein coding sequence of done yf33_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yf33_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yf33_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:174 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:174, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:174 having biological activity, the fragment comprising the amino acid sequence from amino acid 57 to amino acid 66 of SEQ ID NO:174.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:173.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:173, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:173; and

(ab) the nucleotide sequence of the cDNA insert of done yf33_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:173, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:173; and

(bb) the nucleotide sequence of the cDNA insert of clone yf33_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:173, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:173 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:173, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:173. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:173 from nucleotide 1251 to nucleotide 1625, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:173 from nucleotide 1251 to nucleotide 1625, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:173 from nucleotide 1251 to nucleotide 1625. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:173 from nucleotide 1395 to nucleotide 1625, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:173 from nucleotide 1395 to nucleotide 1625, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:173 from nucleotide 1395 to nucleotide 1625.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:174;

(b) a fragment of the amino acid sequence of SEQ ID NO:174, the fragment comprising eight contiguous amino acids of SEQ ID NO:174; and

(c) the amino acid sequence encoded by the cDNA insert of clone yf33_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:174. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:174 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:174, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:174 having biological activity, the fragment comprising the amino acid sequence from amino acid 57 to amino acid 66 of SEQ ID NO:174.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:175;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:175 from nucleotide 1299 to nucleotide 1640;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yi15_(—)1 deposited under accession number ATCC 98924;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi15_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi15_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi15_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:176;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:176 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:176;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:175.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:175 from nucleotide 1299 to nucleotide 1640; the nucleotide sequence of the full-length protein coding sequence of clone yi15_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yi15_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi15_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:176 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:176, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:176 having biological activity, the fragment comprising the amino acid sequence from amino acid 52 to amino acid 61 of SEQ ID NO:176.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:175.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:175, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:175; and

(ab) the nucleotide sequence of the cDNA insert of clone yi15_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:175, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:175; and

(bb) the nucleotide sequence of the cDNA insert of clone yi15_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:175, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:175 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:175, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:175. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:175 from nucleotide 1299 to nucleotide 1640, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:175 from nucleotide 1299 to nucleotide 1640, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:175 from nucleotide 1299 to nucleotide 1640.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:176;

(b) a fragment of the amino acid sequence of SEQ ID NO:176, the fragment comprising eight contiguous amino acids of SEQ ID NO:176; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi15_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:176. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:176 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:176, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:176 having biological activity, the fragment comprising the amino acid sequence from amino acid 52 to amino acid 61 of SEQ ID NO:176.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:177;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:177 from nucleotide 85 to nucleotide 1377;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:177 from nucleotide 139 to nucleotide 1377;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of done yi17_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi17_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi17_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi17_(—)1 deposited under accession number ATCC 98924;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:178;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:178 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:178;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:177.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:177 from nucleotide 85 to nucleotide 1377; the nucleotide sequence of SEQ ID NO:177 from nucleotide 139 to nucleotide 1377; the nucleotide sequence of the full-length protein coding sequence of clone yi17_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yi17_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi17_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:178 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:178, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:178 having biological activity, the fragment comprising the amino acid sequence from amino acid 210 to amino acid 219 of SEQ ID NO:178.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:177.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:177, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:177; and

(ab) the nucleotide sequence of the cDNA insert of clone yi17_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:177, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:177; and

(bb) the nucleotide sequence of the cDNA insert of clone yi17_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:177, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:177 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:177, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:177. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:177 from nucleotide 85 to nucleotide 1377, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:177 from nucleotide 85 to nucleotide 1377, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:177 from nucleotide 85 to nucleotide 1377. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:177 from nucleotide 139 to nucleotide 1377, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:177 from nucleotide 139 to nucleotide 1377, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:177 from nucleotide 139 to nucleotide 1377.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:178;

(b) a fragment of the amino acid sequence of SEQ ID NO:178, the fragment comprising eight contiguous amino acids of SEQ ID NO:178; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi17_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:178. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:178 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:178, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:178 having biological activity, the fragment comprising the amino acid sequence from amino acid 210 to amino acid 219 of SEQ ID NO:178.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:179;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:179 from nucleotide 50 to nucleotide 1075;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:179 from nucleotide 215 to nucleotide 1075;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk38_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk38_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk38_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk38_(—)1 deposited under accession number ATCC 98924;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:180;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:180 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:180;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:179.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:179 from nucleotide 50 to nucleotide 1075; the nucleotide sequence of SEQ ID NO:179 from nucleotide 215 to nucleotide 1075; the nucleotide sequence of the full-length protein coding sequence of clone yk38_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yk38_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk38_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:180 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:180, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:180 having biological activity, the fragment comprising the amino acid sequence from amino acid 166 to amino acid 175 of SEQ ID NO:180.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:179.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:179, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:179; and

(ab) the nucleotide sequence of the cDNA insert of clone yk38_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:179, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:179; and

(bb) the nucleotide sequence of the cDNA insert of clone yk38_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:179, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:179 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:179, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:179. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:179 from nucleotide 50 to nucleotide 1075, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:179 from nucleotide 50 to nucleotide 1075, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:179 from nucleotide 50 to nucleotide 1075. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:179 from nucleotide 215 to nucleotide 1075, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:179 from nucleotide 215 to nucleotide 1075, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:179 from nucleotide 215 to nucleotide 1075.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:180;

(b) a fragment of the amino acid sequence of SEQ ID NO:180, the fragment comprising eight contiguous amino acids of SEQ ID NO:180; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk38_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:180. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:180 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:180, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:180 having biological activity, the fragment comprising the amino acid sequence from amino acid 166 to amino acid 175 of SEQ ID NO:180.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:181;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:181 from nucleotide 76 to nucleotide 348;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:181 from nucleotide 139 to nucleotide 348;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk51_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk51_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk51_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk51_(—)1 deposited under accession number ATCC 98924;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:182;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:182 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:182;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:181.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:181 from nucleotide 76 to nucleotide 348; the nucleotide sequence of SEQ ID NO:181 from nucleotide 139 to nucleotide 348; the nucleotide sequence of the full-length protein coding sequence of clone yk51_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yk51_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk51_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:182 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:182, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:182 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:182.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:181.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:181, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:181; and

(ab) the nucleotide sequence of the cDNA insert of clone yk51_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:181, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:181; and

(bb) the nucleotide sequence of the cDNA insert of clone yk51_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:181, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:181 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:181, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:181. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:181 from nucleotide 76 to nucleotide 348, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:181 from nucleotide 76 to nucleotide 348, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:181 from nucleotide 76 to nucleotide 348. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:181 from nucleotide 139 to nucleotide 348, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:181 from nucleotide 139 to nucleotide 348, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:181 from nucleotide 139 to nucleotide 348.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:182;

(b) a fragment of the amino acid sequence of SEQ ID NO:182, the fragment comprising eight contiguous amino acids of SEQ ID NO:182; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk51_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:182. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:182 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:182, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:182 having biological activity, the fragment comprising the amino acid sequence from amino acid 40 to amino acid 49 of SEQ ID NO:182.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:183;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:183 from nucleotide 203 to nucleotide 577;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk74_(—)1 deposited under accession number ATCC 98924;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk74_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk74_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk74_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:184;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:184 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:184;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:183.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:183 from nucleotide 203 to nucleotide 577; the nucleotide sequence of the full-length protein coding sequence of clone yk74_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yk74_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk74_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:184 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:184, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:184 having biological activity, the fragment comprising the amino acid sequence from amino acid 57 to amino acid 66 of SEQ ID NO:184.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:183.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:183, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:183; and

(ab) the nucleotide sequence of the cDNA insert of clone yk74_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:183, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:183; and

(bb) the nucleotide sequence of the cDNA insert of clone yk74_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:183, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:183 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:183, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:183. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:183 from nucleotide 203 to nucleotide 577, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:183 from nucleotide 203 to nucleotide 577, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:183 from nucleotide 203 to nucleotide 577.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:184;

(b) a fragment of the amino acid sequence of SEQ ID NO:184, the fragment comprising eight contiguous amino acids of SEQ ID NO:184; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk74_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:184. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:184 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:184, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:184 having biological activity, the fragment comprising the amino acid sequence from amino acid 57 to amino acid 66 of SEQ ID NO:184.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:185;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:185 from nucleotide 38 to nucleotide 2170;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk89_(—)1 deposited under accession number ATCC 98924;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk89_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk89_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk89_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:186;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:186 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:186;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:185.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:185 from nucleotide 38 to nucleotide 2170; the nucleotide sequence of the full-length protein coding sequence of clone yk89_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yk89_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk89_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:186 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:186, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:186 having biological activity, the fragment comprising the amino acid sequence from amino acid 350 to amino acid 359 of SEQ ID NO:186.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:185.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:185, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:185; and

(ab) the nucleotide sequence of the cDNA insert of clone yk89_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:185, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:185; and

(bb) the nucleotide sequence of the cDNA insert of clone yk89_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:185, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:185 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:185, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:185. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:185 from nucleotide 38 to nucleotide 2170, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:185 from nucleotide 38 to nucleotide 2170, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:185 from nucleotide 38 to nucleotide 2170.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:186;

(b) a fragment of the amino acid sequence of SEQ ID NO:186, the fragment comprising eight contiguous amino acids of SEQ ID NO:186; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk89_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:186. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:186 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:186, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:186 having biological activity, the fragment comprising the amino acid sequence from amino acid 350 to amino acid 359 of SEQ ID NO:186.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:187;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:187 from nucleotide 14 to nucleotide 742;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:187 from nucleotide 89 to nucleotide 742;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of done yl18_(—)1 deposited under accession number ATCC 98924;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yl18_(—)1 deposited under accession number ATCC 98924;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yl18_(—)1 deposited under accession number ATCC 98924;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yl18_(—)1 deposited under accession number ATCC 98924;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:188;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:188 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:188;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:187.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:187 from nucleotide 14 to nucleotide 742; the nucleotide sequence of SEQ ID NO:187 from nucleotide 89 to nucleotide 742; the nucleotide sequence of the full-length protein coding sequence of clone yl18_(—)1 deposited under accession number ATCC 98924; or the nucleotide sequence of a mature protein coding sequence of clone yl18_(—)1 deposited under accession number ATCC 98924. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yl18_(—)1 deposited under accession number ATCC 98924. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:188 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:188, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:188 having biological activity, the fragment comprising the amino acid sequence from amino acid 116 to amino acid 125 of SEQ ID NO:188.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:187.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:187, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:187; and

(ab) the nucleotide sequence of the cDNA insert of clone yl18_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:187, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:187; and

(bb) the nucleotide sequence of the cDNA insert of clone yl18_(—)1 deposited under accession number ATCC 98924;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:187, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:187 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:187, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:187. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:187 from nucleotide 14 to nucleotide 742, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:187 from nucleotide 14 to nucleotide 742, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:187 from nucleotide 14 to nucleotide 742. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:187 from nucleotide 89 to nucleotide 742, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:187 from nucleotide 89 to nucleotide 742, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:187 from nucleotide 89 to nucleotide 742.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:188;

(b) a fragment of the amino acid sequence of SEQ ID NO:188, the fragment comprising eight contiguous amino acids of SEQ ID NO:188; and

(c) the amino acid sequence encoded by the cDNA insert of clone yl18_(—)1 deposited under accession number ATCC 98924;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:188. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:188 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:188, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:188 having biological activity, the fragment comprising the amino acid sequence from amino acid 116 to amino acid 125 of SEQ ID NO:188.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:189;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:189 from nucleotide 280 to nucleotide 615;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:189 from nucleotide 325 to nucleotide 615;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yb325_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yb325_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yb325_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yb325_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:190;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:190 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:190;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:189.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:189 from nucleotide 280 to nucleotide 615; the nucleotide sequence of SEQ ID NO:189 from nucleotide 325 to nucleotide 615; the nucleotide sequence of the full-length protein coding sequence of clone yb325_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yb325_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yb325_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:190 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:190, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:190 having biological activity, the fragment comprising the amino acid sequence from amino acid 51 to amino acid 60 of SEQ ID NO:190.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:189.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:189; and

(ab) the nucleotide sequence of the cDNA insert of clone yb325_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:189; and

(bb) the nucleotide sequence of the cDNA insert of clone yb325_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:189, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:189 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:189. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:189 from nucleotide 280 to nucleotide 615, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:189 from nucleotide 280 to nucleotide 615, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:189 from nucleotide 280 to nucleotide 615. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:189 from nucleotide 325 to nucleotide 615, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:189 from nucleotide 325 to nucleotide 615, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:189 from nucleotide 325 to nucleotide 615.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:190;

(b) a fragment of the amino acid sequence of SEQ ID NO:190, the fragment comprising eight contiguous amino acids of SEQ ID NO:190; and

(c) the amino acid sequence encoded by the cDNA insert of clone yb325_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:190. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:190 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:190, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:190 having biological activity, the fragment comprising the amino acid sequence from amino acid 51 to amino acid 60 of SEQ ID NO:190.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:191;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:191 from nucleotide 163 to nucleotide 429;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:191 from nucleotide 274 to nucleotide 429;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yd261_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yd261_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yd261_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yd261_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:192;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:192 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:192;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:191.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:191 from nucleotide 163 to nucleotide 429; the nucleotide sequence of SEQ ID NO:191 from nucleotide 274 to nucleotide 429; the nucleotide sequence of the full-length protein coding sequence of clone yd261_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yd261_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yd261_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:192 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:192, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:192 having biological activity, the fragment comprising the amino acid sequence from amino acid 39 to amino acid 48 of SEQ ID NO:192.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:191.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:191, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:191; and

(ab) the nucleotide sequence of the cDNA insert of clone yd261_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:191, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:191; and

(bb) the nucleotide sequence of the cDNA insert of clone yd261_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:191, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:191 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:191, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:191. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:191 from nucleotide 163 to nucleotide 429, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:191 from nucleotide 163 to nucleotide 429, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:191 from nucleotide 163 to nucleotide 429. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:191 from nucleotide 274 to nucleotide 429, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:191 from nucleotide 274 to nucleotide 429, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:191 from nucleotide 274 to nucleotide 429.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:192;

(b) a fragment of the amino acid sequence of SEQ ID NO:192, the fragment comprising eight contiguous amino acids of SEQ ID NO:192; and

(c) the amino acid sequence encoded by the cDNA insert of clone yd261_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:192. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:192 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:192, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:192 having biological activity, the fragment comprising the amino acid sequence from amino acid 39 to amino acid 48 of SEQ ID NO:192.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:193;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:193 from nucleotide 1262 to nucleotide 1858;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yh33_(—)1 deposited under accession number ATCC 98958;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yh33_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yh33_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yh33_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:194;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:194 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:194;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:193.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:193 from nucleotide 1262 to nucleotide 1858; the nucleotide sequence of the full-length protein coding sequence of clone yh33_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yh33_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yh33_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:194 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:194, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:194 having biological activity, the fragment comprising the amino acid sequence from amino acid 94 to amino acid 103 of SEQ ID NO:194.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:193.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:193, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:193; and

(ab) the nucleotide sequence of the cDNA insert of clone yh33_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:193, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:193; and

(bb) the nucleotide sequence of the cDNA insert of clone yh33_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:193, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:193 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:193, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:193. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:193 from nucleotide 1262 to nucleotide 1858, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:193 from nucleotide 1262 to nucleotide 1858, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:193 from nucleotide 1262 to nucleotide 1858.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:194;

(b) a fragment of the amino acid sequence of SEQ ID NO:194, the fragment comprising eight contiguous amino acids of SEQ ID NO:194; and

(c) the amino acid sequence encoded by the cDNA insert of clone yh33_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:194. In further preferred embodiments; the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:194 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:194, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:194 having biological activity, the fragment comprising the amino acid sequence from amino acid 94 to amino acid 103 of SEQ ID NO:194.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:195;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:195 from nucleotide 25 to nucleotide 1851;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:195 from nucleotide 250 to nucleotide 1851;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yi16_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yi16_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yi16_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yi16_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:196;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:196 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:196;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:195.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:195 from nucleotide 25 to nucleotide 1851; the nucleotide sequence of SEQ ID NO:195 from nucleotide 250 to nucleotide 1851; the nucleotide sequence of the full-length protein coding sequence of clone yi16_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yi16_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yi16_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:196 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:196, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:196 having biological activity, the fragment comprising the amino acid sequence from amino acid 299 to amino acid 308 of SEQ ID NO:196.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:195.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:195, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:195; and

(ab) the nucleotide sequence of the cDNA insert of clone yi16_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:195, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:195; and

(bb) the nucleotide sequence of the cDNA insert of clone yi16_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:195, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:195 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:195, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:195. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:195 from nucleotide 25 to nucleotide 1851, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:195 from nucleotide 25 to nucleotide 1851, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:195 from nucleotide to nucleotide 1851. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:195 from nucleotide 250 to nucleotide 1851, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:195 from nucleotide 250 to nucleotide 1851, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:195 from nucleotide 250 to nucleotide 1851.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:196;

(b) a fragment of the amino acid sequence of SEQ ID NO:196, the fragment comprising eight contiguous amino acids of SEQ ID NO:196; and

(c) the amino acid sequence encoded by the cDNA insert of clone yi16_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:196. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:196 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:196, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:196 having biological activity, the fragment comprising the amino acid sequence from amino acid 299 to amino acid 308 of SEQ ID NO:196.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:197;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:197 from nucleotide 739 to nucleotide 996;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk46_(—)1 deposited under accession number ATCC 98958;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk46_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk46_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk46_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:198;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:198 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:198;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:197.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:197 from nucleotide 739 to nucleotide 996; the nucleotide sequence of the full-length protein coding sequence of clone yk46_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk46_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk46_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:198 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:198, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:198 having biological activity, the fragment comprising the amino acid sequence from amino acid 38 to amino acid 47 of SEQ ID NO:198.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:197.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:197, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:197; and

(ab) the nucleotide sequence of the cDNA insert of clone yk46_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:197, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:197; and

(bb) the nucleotide sequence of the cDNA insert of clone yk46_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:197, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:197 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:197, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:197. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:197 from nucleotide 739 to nucleotide 996, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:197 from nucleotide 739 to nucleotide 996, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:197 from nucleotide 739 to nucleotide 996.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:198;

(b) a fragment of the amino acid sequence of SEQ ID NO:198, the fragment comprising eight contiguous amino acids of SEQ ID NO:198; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk46_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:198. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:198 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:198, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:198 having biological activity, the fragment comprising the amino acid sequence from amino acid 38 to amino acid 47 of SEQ ID NO:198.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:199;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:199 from nucleotide 222 to nucleotide 605;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:199 from nucleotide 366 to nucleotide 605;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk84_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk84_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk84_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk84_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:200;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:200 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:200;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:199.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:199 from nucleotide 222 to nucleotide 605; the nucleotide sequence of SEQ ID NO:199 from nucleotide 366 to nucleotide 605; the nucleotide sequence of the full-length protein coding sequence of clone yk84_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk84_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk84_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:200 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:200, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:200 having biological activity, the fragment comprising the amino acid sequence from amino acid 59 to amino acid 68 of SEQ ID NO:200.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:199.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:199, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:199; and

(ab) the nucleotide sequence of the cDNA insert of clone yk84_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:199, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:199; and

(bb) the nucleotide sequence of the cDNA insert of clone yk84_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:199, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:199 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:199, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:199. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:199 from nucleotide 222 to nucleotide 605, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:199 from nucleotide 222 to nucleotide 605, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:199 from nucleotide 222 to nucleotide 605. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:199 from nucleotide 366 to nucleotide 605, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:199 from nucleotide 366 to nucleotide 605, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:199 from nucleotide 366 to nucleotide 605.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:200;

(b) a fragment of the amino acid sequence of SEQ ID NO:200, the fragment comprising eight contiguous amino acids of SEQ ID NO:200; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk84_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:200. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:200 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:200, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:200 having biological activity, the fragment comprising the amino acid sequence from amino acid 59 to amino acid 68 of SEQ ID NO:200.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:201;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:201 from nucleotide 140 to nucleotide 1036;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:201 from nucleotide 269 to nucleotide 1036;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk143_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk143_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk143_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk143_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:202;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:202 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:202;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:201.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:201 from nucleotide 140 to nucleotide 1036; the nucleotide sequence of SEQ ID NO:201 from nucleotide 269 to nucleotide 1036; the nucleotide sequence of the full-length protein coding sequence of clone yk143_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk143_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk143_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:202 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:202, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:202 having biological activity, the fragment comprising the amino acid sequence from amino acid 144 to amino acid 153 of SEQ ID NO:202.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:201.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:201, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:201; and

(ab) the nucleotide sequence of the cDNA insert of clone yk143_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:201, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:201; and

(bb) the nucleotide sequence of the cDNA insert of clone yk143_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:201, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:201 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:201, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:201. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:201 from nucleotide 140 to nucleotide 1036, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:201 from nucleotide 140 to nucleotide 1036, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:201 from nucleotide 140 to nucleotide 1036. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:201 from nucleotide 269 to nucleotide 1036, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:201 from nucleotide 269 to nucleotide 1036, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:201 from nucleotide 269 to nucleotide 1036.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:202;

(b) a fragment of the amino acid sequence of SEQ ID NO:202, the fragment comprising eight contiguous amino acids of SEQ ID NO:202; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk143_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:202. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:202 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:202, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:202 having biological activity, the fragment comprising the amino acid sequence from amino acid 144 to amino acid 153 of SEQ ID NO:202.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:203;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:203 from nucleotide 304 to nucleotide 636;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:203 from nucleotide 415 to nucleotide 636;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk156_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk156_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk156_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk156_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:204;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:204 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:204;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:203.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:203 from nucleotide 304 to nucleotide 636; the nucleotide sequence of SEQ ID NO:203 from nucleotide 415 to nucleotide 636; the nucleotide sequence of the full-length protein coding sequence of clone yk156_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk156_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk156_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:204 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:204, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:204 having biological activity, the fragment comprising the amino acid sequence from amino acid 50 to amino acid 59 of SEQ ID NO:204.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:203.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:203, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:203; and

(ab) the nucleotide sequence of the cDNA insert of clone yk156_(—)1 deposited under accession number ATCC 98958;

(i) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:203, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:203; and

(bb) the nucleotide sequence of the cDNA insert of clone yk156_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:203, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:203 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:203 but excluding the poly(A) tail at the 3′ end of SEQ ID NO:203. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:203 from nucleotide 304 to nucleotide 636, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:203 from nucleotide 304 to nucleotide 636, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:203 from nucleotide 304 to nucleotide 636. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:203 from nucleotide 415 to nucleotide 636, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:203 from nucleotide 415 to nucleotide 636, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:203 from nucleotide 415 to nucleotide 636.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:204;

(b) a fragment of the amino acid sequence of SEQ ID NO:204, the fragment comprising eight contiguous amino acids of SEQ ID NO:204; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk156_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:204. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:204 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:204, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:204 having biological activity, the fragment comprising the amino acid sequence from amino acid 50 to amino acid 59 of SEQ ID NO:204.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:205;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:205 from nucleotide 571 to nucleotide 891;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:205 from nucleotide 745 to nucleotide 891;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk204_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk204_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk204_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk204_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:206;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:206 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:206;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:205.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:205 from nucleotide 571 to nucleotide 891; the nucleotide sequence of SEQ ID NO:205 from nucleotide 745 to nucleotide 891; the nucleotide sequence of the full-length protein coding sequence of clone yk204_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk204_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk204_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:206 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:206, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:206 having biological activity, the fragment comprising the amino acid sequence from amino acid 48 to amino acid 57 of SEQ ID NO:206.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:205.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:205, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:205; and

(ab) the nucleotide sequence of the cDNA insert of clone yk204_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(j) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:205, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:205; and

(bb) the nucleotide sequence of the cDNA insert of clone yk204_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:205, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:205 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:205, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:205. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:205 from nucleotide 571 to nucleotide 891, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:205 from nucleotide 571 to nucleotide 891, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:205 from nucleotide 571 to nucleotide 891. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:205 from nucleotide 745 to nucleotide 891, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:205 from nucleotide 745 to nucleotide 891, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:205 from nucleotide 745 to nucleotide 891.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:206;

(b) a fragment of the amino acid sequence of SEQ ID NO:206, the fragment comprising eight contiguous amino acids of SEQ ID NO:206; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk204_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:206. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:206 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:206, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:206 having biological activity, the fragment comprising the amino acid sequence from amino acid 48 to amino acid 57 of SEQ ID NO:206.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:207;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:207 from nucleotide 283 to nucleotide 1560;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk224_(—)1 deposited under accession number ATCC 98958;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk224_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk224_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk224_(—)1 deposited under accession number ATCC 98958;,

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:208;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:208 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:208;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:207.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:207 from nucleotide 283 to nucleotide 1560; the nucleotide sequence of the full-length protein coding sequence of clone yk224_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk224_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of done yk224_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:208 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:208, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:208 having biological activity, the fragment comprising the amino acid sequence from amino acid 208 to amino acid 217 of SEQ ID NO:208.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:207.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:207, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:207; and

(ab) the nucleotide sequence of the cDNA insert of clone yk224_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:207, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:207; and

(bb) the nucleotide sequence of the cDNA insert of clone yk224_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:207, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:207 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:207, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:207. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:207 from nucleotide 283 to nucleotide 1560, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:207 from nucleotide 283 to nucleotide 1560, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:207 from nucleotide 283 to nucleotide 1560.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:208;

(b) a fragment of the amino acid sequence of SEQ ID NO:208, the fragment comprising eight contiguous amino acids of SEQ ID NO:208; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk224_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:208. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:208 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:208, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:208 having biological activity, the fragment comprising the amino acid sequence from amino acid 208 to amino acid 217 of SEQ ID NO:208.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:209;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:209 from nucleotide 485 to nucleotide 1465;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:209 from nucleotide 560 to nucleotide 1465;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone yk261_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone yk261_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone yk261_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone yk261_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:210;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:210 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:210;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:209.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:209 from nucleotide 485 to nucleotide 1465; the nucleotide sequence of SEQ ID NO:209 from nucleotide 560 to nucleotide 1465; the nucleotide sequence of the full-length protein coding sequence of clone yk261_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone yk261_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone yk261_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:210 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:210, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:210 having biological activity, the fragment comprising the amino acid sequence from amino acid 158 to amino acid 167 of SEQ ID NO:210.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:209.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:209, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:209; and

(ab) the nucleotide sequence of the cDNA insert of clone yk261_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:209, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:209; and

(bb) the nucleotide sequence of the cDNA insert of clone yk261_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:209, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:209 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:209, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:209. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:209 from nucleotide 485 to nucleotide 1465, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:209 from nucleotide 485 to nucleotide 1465, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:209 from nucleotide 485 to nucleotide 1465. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:209 from nucleotide 560 to nucleotide 1465, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:209 from nucleotide 560 to nucleotide 1465, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:209 from nucleotide 560 to nucleotide 1465.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:210;

(b) a fragment of the amino acid sequence of SEQ ID NO:210, the fragment comprising eight contiguous amino acids of SEQ ID NO:210; and

(c) the amino acid sequence encoded by the cDNA insert of clone yk261_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:210. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:210 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:210, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:210 having biological activity, the fragment comprising the amino acid sequence from amino acid 158 to amino acid 167 of SEQ ID NO:210.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:211;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:211 from nucleotide 96 to nucleotide 821;

(c) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ys3_(—)1 deposited under accession number ATCC 98958;

(d) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ys3_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ys3_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ys3_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:212;

(h) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:212 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:212;

(i) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(f) above;

(j) a polynucleotide which encodes a species homologue of the protein of (g) or (h) above;

(k) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h); and

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(h) and that has a length that is at least 25% of the length of SEQ ID NO:211.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:211 from nucleotide 96 to nucleotide 821; the nucleotide sequence of the full-length protein coding sequence of clone ys3_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone ys3_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ys3_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:212 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:212, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:212 having biological activity, the fragment comprising the amino acid sequence from amino acid 116 to amino acid 125 of SEQ ID NO:212.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:211.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:211, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:211; and

(ab) the nucleotide sequence of the cDNA insert of clone ys3_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:211, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:211; and

(bb) the nucleotide sequence of the cDNA insert of clone y53_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:211, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:211 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:211, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:211. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:211 from nucleotide 96 to nucleotide 821, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:211 from nucleotide 96 to nucleotide 821, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:211 from nucleotide 96 to nucleotide 821.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:212;

(b) a fragment of the amino acid sequence of SEQ ID NO:212, the fragment comprising eight contiguous amino acids of SEQ ID NO:212; and

(c) the amino acid sequence encoded by the cDNA insert of clone ys3_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:212. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:212 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:212, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:212 having biological activity, the fragment comprising the amino acid sequence from amino acid 116 to amino acid 125 of SEQ ID NO:212.

In one embodiment, the present invention provides a composition comprising an isolated polynucleotide selected from the group consisting of:

(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:213;

(b) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:213 from nucleotide 191 to nucleotide 499;

(c) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:213 from nucleotide 317 to nucleotide 499;

(d) a polynucleotide comprising the nucleotide sequence of the full-length protein coding sequence of clone ys10_(—)1 deposited under accession number ATCC 98958;

(e) a polynucleotide encoding the full-length protein encoded by the cDNA insert of clone ys10_(—)1 deposited under accession number ATCC 98958;

(f) a polynucleotide comprising the nucleotide sequence of a mature protein coding sequence of clone ys10_(—)1 deposited under accession number ATCC 98958;

(g) a polynucleotide encoding a mature protein encoded by the cDNA insert of clone ys10_(—)1 deposited under accession number ATCC 98958;

(h) a polynucleotide encoding a protein comprising the amino acid sequence of SEQ ID NO:214;

(i) a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:214 having biological activity, the fragment comprising eight contiguous amino acids of SEQ ID NO:214;

(j) a polynucleotide which is an allelic variant of a polynucleotide of (a)-(g) above;

(k) a polynucleotide which encodes a species homologue of the protein of (h) or (i) above;

(l) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i); and

(m) a polynucleotide that hybridizes under stringent conditions to any one of the polynucleotides specified in (a)-(i) and that has a length that is at least 25% of the length of SEQ ID NO:213.

Preferably, such polynucleotide comprises the nucleotide sequence of SEQ ID NO:213 from nucleotide 191 to nucleotide 499; the nucleotide sequence of SEQ ID NO:213 from nucleotide 317 to nucleotide 499; the nucleotide sequence of the full-length protein coding sequence of clone ys10_(—)1 deposited under accession number ATCC 98958; or the nucleotide sequence of a mature protein coding sequence of clone ys10_(—)1 deposited under accession number ATCC 98958. In other preferred embodiments, the polynucleotide encodes the full-length or a mature protein encoded by the cDNA insert of clone ys10_(—)1 deposited under accession number ATCC 98958. In further preferred embodiments, the present invention provides a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:214 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:214, or a polynucleotide encoding a protein comprising a fragment of the amino acid sequence of SEQ ID NO:214 having biological activity, the fragment comprising the amino acid sequence from amino acid 46 to amino acid 55 of SEQ ID NO:214.

Other embodiments provide the gene corresponding to the cDNA sequence of SEQ ID NO:213.

Further embodiments of the invention provide isolated polynucleotides produced according to a process selected from the group consisting of:

(a) a process comprising the steps of:

(i) preparing one or more polynucleotide probes that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(aa) SEQ ID NO:213, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:213; and

(ab) the nucleotide sequence of the cDNA insert of clone ys10_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said probe(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.; and

(iii) isolating the DNA polynucleotides detected with the probe(s);

and

(b) a process comprising the steps of:

(i) preparing one or more polynucleotide primers that hybridize in 6×SSC at 65 degrees C. to a nucleotide sequence selected from the group consisting of:

(ba) SEQ ID NO:213, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:213; and

(bb) the nucleotide sequence of the cDNA insert of clone ys10_(—)1 deposited under accession number ATCC 98958;

(ii) hybridizing said primer(s) to human genomic DNA in conditions at least as stringent as 4×SSC at 50 degrees C.;

(iii) amplifying human DNA sequences; and

(iv) isolating the polynucleotide products of step (b)(iii).

Preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:213, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of SEQ ID NO:213 to a nucleotide sequence corresponding to the 3′ end of SEQ ID NO:213, but excluding the poly(A) tail at the 3′ end of SEQ ID NO:213. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:213 from nucleotide 191 to nucleotide 499, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:213 from nucleotide 191 to nucleotide 499, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:213 from nucleotide 191 to nucleotide 499. Also preferably the polynucleotide isolated according to the above process comprises a nucleotide sequence corresponding to the cDNA sequence of SEQ ID NO:213 from nucleotide 317 to nucleotide 499, and extending contiguously from a nucleotide sequence corresponding to the 5′ end of said sequence of SEQ ID NO:213 from nucleotide 317 to nucleotide 499, to a nucleotide sequence corresponding to the 3′ end of said sequence of SEQ ID NO:213 from nucleotide 317 to nucleotide 499.

In other embodiments, the present invention provides a composition comprising a protein, wherein said protein comprises an amino acid sequence selected from the group consisting of:

(a) the amino acid sequence of SEQ ID NO:214;

(b) a fragment of the amino acid sequence of SEQ ID NO:214, the fragment comprising eight contiguous amino acids of SEQ ID NO:214; and

(c) the amino acid sequence encoded by the cDNA insert of clone ys10_(—)1 deposited under accession number ATCC 98958;

the protein being substantially free from other mammalian proteins. Preferably such protein comprises the amino acid sequence of SEQ ID NO:214. In further preferred embodiments, the present invention provides a protein comprising a fragment of the amino acid sequence of SEQ ID NO:214 having biological activity, the fragment preferably comprising eight (more preferably twenty, most preferably thirty) contiguous amino acids of SEQ ID NO:214, or a protein comprising a fragment of the amino acid sequence of SEQ ID NO:214 having biological activity, the fragment comprising the amino acid sequence from amino acid 46 to amino acid 55 of SEQ ID NO:214.

In certain preferred embodiments, the polynucleotide is operably linked to an expression control sequence. The invention also provides a host cell, including bacterial, yeast, insect and mammalian cells, transformed with such polynucleotide compositions. Also provided by the present invention are organisms that have enhanced, reduced, or modified expression of the gene(s) corresponding to the polynucleotide sequences disclosed herein.

Processes are also provided for producing a protein, which comprise:

(a) growing a culture of the host cell transformed with such polynucleotide compositions in a suitable culture medium; and

(b) purifying the protein from the culture.

The protein produced according to such methods is also provided by the present invention.

Protein compositions of the present invention may further comprise a pharmaceutically acceptable carrier. Compositions comprising an antibody which specifically reacts with such protein are also provided by the present invention.

Methods are also provided for preventing, treating or ameliorating a medical condition which comprises administering to a mammalian subject a therapeutically effective amount of a composition comprising a protein of the present invention and a pharmaceutically acceptable carrier.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B are schematic representations of the pED6 and pNOTs vectors, respectively, used for deposit of clones disclosed herein.

DETAILED DESCRIPTION

ISOLATED PROTEINS AND POLYNUCLEOTIDES

Nucleotide and amino acid sequences, as presently determined, are reported below for each clone and protein disclosed in the present application. The nucleotide sequence of each clone can readily be determined by sequencing of the deposited clone in accordance with known methods. The predicted amino acid sequence (both full-length and mature forms) can then be determined from such nucleotide sequence. The amino acid sequence of the protein encoded by a particular clone can also be determined by expression of the clone in a suitable host cell, collecting the protein and determining its sequence. For each disclosed protein applicants have identified what they have determined to be the reading frame best identifiable with sequence information available at the time of filing.

As used herein a “secreted” protein is one which, when expressed in a suitable host cell, is transported across or through a membrane, including transport as a result of signal sequences in its amino acid sequence. “Secreted” proteins include without limitation proteins secreted wholly (e.g., soluble proteins) or partially (e.g., receptors) from the cell in which they are expressed. “Secreted” proteins also include without limitation proteins which are transported across the membrane of the endoplasmic reticulum.

Clone “ya15_(—)1”

A polynucleotide of the present invention has been identified as clone “ya15_(—)1”. ya15_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya15_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya15_(—)1 protein”).

The nucleotide sequence of ya15_(—)1 as presently determined is reported in SEQ ID NO:1, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya15_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:2. Amino acids 8 to 20 of SEQ ID NO:2 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 21. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya15_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya15_(—)1 should be approximately 1100 bp.

The nucleotide sequence disclosed herein for ya15_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya15_(—)1 demonstrated at least some similarity with sequences identified as Z94056 (Human DNA sequence from PAC 436M11 on chromosome Xp22.11-22.2; contains a serine threonine protein phosphatase gene, ESTs and STSs). Based upon sequence similarity, ya15_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the ya15_(—)1 protein sequence centered around amino acid 40 of SEQ ID NO:2. The nucleotide sequence of ya15_(—)1 indicates that it may contain an Alu repetitive element.

Clone “ya24_(—)1”

A polynucleotide of the present invention has been identified as clone “ya24_(—)1”. ya24_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya24_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya24_(—)1 protein”).

The nucleotide sequence of ya24_(—)1 as presently determined is reported in SEQ ID NO:3, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya24_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:4. Amino acids 3 to 15 of SEQ ID NO:4 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 16. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya24_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya24_(—)1 should be approximately 750 bp.

The nucleotide sequence disclosed herein for ya24_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya24_(—)1 demonstrated at least some similarity with sequences identified as AA537299 (vk46d03.r1 Soares mouse mammary gland NbMMG Mus musculus cDNA clone 949637 5′). Based upon sequence similarity, ya24_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yb42_(—)1”

A polynucleotide of the present invention has been identified as clone “yb42_(—)1”. yb42_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb42_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb42_(—)1 protein”).

The nucleotide sequence of yb42_(—)1 as presently determined is reported in SEQ ID NO:5, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb42_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:6. Amino acids 41 to 53 of SEQ ID NO:6 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 54. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb42_(—)1 protein.

Another potential yb42_(—)1 reading frame and predicted amino acid sequence is encoded by basepairs 1879 to 2220 of SEQ ID NO:5 and is reported in SEQ ID NO:265; amino acids 54 to 66 of SEQ ID NO:265 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 67 of SEQ ID NO:265. Due to the hydrophobic nature of this predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the protein of SEQ ID NO:265.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb42_(—)1 should be approximately 3900 bp.

The nucleotide sequence disclosed herein for yb42_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb42_(—)1 demonstrated at least some similarity with sequences identified as AA213992 (zn58d08.s1 Stratagene muscle 937209 Homo sapiens cDNA clone 562383 3′). Based upon sequence similarity, yb42_(—)1 proteins and each similar protein or peptide may share at least some activity. The nucleotide sequence of yb42_(—)1 indicates that it may contain at least one MIR repeat sequence.

Clone “yc9_(—)1”

A polynucleotide of the present invention has been identified as clone “yc9_(—)1”. yc9_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc9_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc9_(—)1 protein”).

The nucleotide sequence of yc9_(—)1 as presently determined is reported in SEQ ID NO:7, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc9_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:8.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc9_(—)1 should be approximately 3300 bp.

The nucleotide sequence disclosed herein for yc9_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc9_(—)1 demonstrated at least some similarity with sequences identified as AA588539 (nm94a07.s1 NCI_CGAP_Co9 Homo sapiens cDNA clone IMAGE:1075860) and N47418 (yy88e12.r1 Homo sapiens cDNA clone 280654 5′). The predicted amino acid sequence disclosed herein for yc9_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yc9_(—)1 protein demonstrated at least some similarity to sequences identified as X97196 (D. melanogaster X gene). Based upon sequence similarity, yc9_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yc9_(—)1 protein sequence, centered around amino acids 80 and 200 of SEQ ID NO:8, respectively.

Clone “yc19_(—)1”

A polynucleotide of the present invention has been identified as clone “yc19_(—)1”. yc19_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc19_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc19_(—)1 protein”).

The nucleotide sequence of yc19_(—)1 as presently determined is reported in SEQ ID NO:9, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc19_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:10. Amino acids 106 to 118 of SEQ ID NO:10 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 119. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc19_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc19_(—)1 should be approximately 1400 bp.

The nucleotide sequence disclosed herein for yc19_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc19_(—)1 demonstrated at least some similarity with sequences identified as AA126002 (zl85a08.s1 Stratagene colon (#937204) Homo sapiens cDNA clone 511382 3′) and AA307000 (EST177917 Colon carcinoma (HCC) cell line Homo sapiens cDNA 5′ end). The predicted amino acid sequence disclosed herein for yc19_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yc19_(—)1 protein demonstrated at least some similarity to sequences identified as X83742 (MAP kinase phosphotase [Xenopus laevis]), and to several tyrosine phosphatases from other species. Based upon sequence similarity, yc19_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yc19_(—)1 protein sequence centered around amino acid 43 of SEQ ID NO:10; this region (amino acids 30 to 42 of SEQ ID NO:10) may also be a leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 43.

yc19_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in conditioned medium and membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yc20_(—)1”

A polynucleotide of the present invention has been identified as clone “yc20_(—)1”. yc20_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc20_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc20_(—)1 protein”).

The nucleotide sequence of yc20_(—)1 as presently determined is reported in SEQ ID NO:11, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc20_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:12.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc20_(—)1 should be approximately 1450 bp.

The nucleotide sequence disclosed herein for yc20_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc20_(—)1 demonstrated at least some similarity with sequences identified as AA447839 (aa18c12.r1 Soares NhHMPu S1 Homo sapiens cDNA clone 813622 5′), N33405 (yy41e10.s1 Homo sapiens cDNA clone 273834 3′), and T19519 (Human gene signature HUMGS00580). Based upon sequence similarity, yc20_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “ya9_(—)1”

A polynucleotide of the present invention has been identified as clone “ya9_(—)1”. ya9_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya9_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya9_(—)1 protein”).

The nucleotide sequence of ya9_(—)1 as presently determined is reported in SEQ ID NO:13, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya9_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:14. Amino acids 15 to 27 of SEQ ID NO:14 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 28. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya9_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya9_(—)1 should be approximately 950 bp.

The nucleotide sequence disclosed herein for ya9_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya9_(—)1 demonstrated at least some similarity with sequences identified as AA442366 (zv62c04.r1 Soares testis NHT Homo sapiens cDNA clone 758214 5′) and AA609166 (af12a08.s1 Soares testis NHT Homo sapiens cDNA clone 1031414 3′). Based upon sequence similarity, ya9_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the ya9_(—)1 protein sequence, centered around amino acid 62 of SEQ ID NO:14.

Clone “ya11_(—)1”

A polynucleotide of the present invention has been identified as clone “ya11_(—)1”. ya11_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya11_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya11_(—)1 protein”).

The nucleotide sequence of ya11_(—)1 as presently determined is reported in SEQ ID NO:15, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya11_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:16. Amino acids 36 to 48 of SEQ ID NO:16 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 49. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya11_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing done ya11_(—)1 should be approximately 500 bp.

The nucleotide sequence disclosed herein for ya11_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya11_(—)1 demonstrated at least some similarity with sequences identified as Z68274 (Human DNA sequence from cosmid L129H7, Huntington's Disease Region, chromosome 4p16.3 contains Pseudogene and CpG island). Based upon sequence similarity, ya11_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the ya11_(—)1 protein sequence, centered around amino acid 81 of SEQ ID NO:16.

Clone “ya28_(—)1”

A polynucleotide of the present invention has been identified as clone “ya28_(—)1”. ya28_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya28_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya28_(—)1 protein”).

The nucleotide sequence of ya28_(—)1 as presently determined is reported in SEQ ID NO:17, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya28_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:18. Amino acids 41 to 53 of SEQ ID NO:18 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 54. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya28_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya28_(—)1 should be approximately 300 bp.

The nucleotide sequence disclosed herein for ya28_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya28_(—)1 demonstrated at least some similarity with sequences identified as AA576255 (nm62b09.s1 NCI_CGAP_Br3 Homo sapiens cDNA clone IMAGE:1072793). Based upon sequence similarity, ya28_(—)1 proteins and each similar protein or peptide may share at least some activity.

ya28_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yb81_(—)1”

A polynucleotide of the present invention has been identified as clone “yb81_(—)1”. yb81_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb81_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb81_(—)1 protein”).

The nucleotide sequence of yb81_(—)1 as presently determined is reported in SEQ ID NO:19, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb81_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:20.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb81_(—)1 should be approximately 1200 bp.

The nucleotide sequence disclosed herein for yb81_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb81_(—)1 demonstrated at least some similarity with sequences identified as T67164 (Human alpha-N-acetylglucosaminidase gene). Based upon sequence similarity, yb81_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yb81_(—)1 protein sequence centered around amino acid 73 of SEQ ID NO:20.

Clone “yc14_(—)1”

A polynucleotide of the present invention has been identified as clone “yc14_(—)1”. yc14_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc14_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc14_(—)1 protein”).

The nucleotide sequence of yc14_(—)1 as presently determined is reported in SEQ ID NO:21, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc14_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:22. Amino acids 388 to 400 of SEQ ID NO:22 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 401. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc14_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc14_(—)1 should be approximately 3000 bp.

The nucleotide sequence disclosed herein for yc14_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc14_(—)1 demonstrated at least some similarity with sequences identified as AA007392 (zh99a08.r1 Soares fetal liver spleen 1NFLS S1 Homo sapiens cDNA clone 429398 5′), AA573120 (nj41e10.s1 NCI_CGAP_AA1 Homo sapiens cDNA clone IMAGE 995082 similar to TR G285999 G285999 ORF, COMPLETE CDS), and D13642 (Human mRNA for KIAA0017 gene, complete cds). The predicted amino acid sequence disclosed herein for yc14_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yc14_(—)1 protein demonstrated at least some similarity to sequences identified as D13642 (KIAA0017 [Homo sapiens]) and Z47816 (unknown [Saccharomyces cerevisiae] (S. cerevisiae chromosome M cosmid 9827, and translated products)). The yc14_(—)1 protein contains the immunoglobulin and major histocompatibility complex protein signature at its extreme N-terminus (starting at amino acid 3 of SEQ ID NO:22). Based upon sequence similarity, yc14_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts four additional potential transmembrane domains within the yc14_(—)1 protein sequence, centered around amino acids 50, 200, 210, and 830 of SEQ ID NO:22, respectively.

yc14_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 92 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yc24_(—)1”

A polynucleotide of the present invention has been identified as clone “yc24_(—)1”. yc24_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc24_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc24_(—)1 protein”).

The nucleotide sequence of yc24_(—)1 as presently determined is reported in SEQ ID NO:23, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc24_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:24. Amino acids 50 to 62 of SEQ ID NO:24 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 63. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc24_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc24_(—)1 should be approximately 1650 bp.

The nucleotide sequence disclosed herein for yc24_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc24_(—)1 demonstrated at least some similarity with sequences identified as AA172170 (zp29b07.s1 Stratagene neuroepithellum (#937231) Homo sapiens cDNA clone 610837 3′ similar to gb L10240 BASIGIN PRECURSOR (HUMAN), AA756004 (vv37a04.r1 Stratagene mouse heart (#937316) Mus musculus cDNA clone 1224558 5′ similar to TR:Q14134 Q14134 ATAXIA-TELANGIECTASIA GROUP D-ASSOCIATED PROTEIN, mRNA sequence), D48379 (Rice cDNA, partial sequence (S145461A), mRNA sequence), E07941 (cDNA encoding human basigin1), L20471 (Human extracellular matrix metalloproteinase inducer gene, complete cds), Q71341 (Human basigin I immunoglobulin gene), and X64364 (H.sapiens mRNA for M6 antigen). The M6 antigen has been localized in all leucocyte lines examined (including lymphocytes, monocytes, and granulocytes) and is implicated in interacting with cytokine factors like GM-CSF and interferon gamma. A protein that is at least very similar to M6 antigen, extracellular matrix metalloproteinase inducer (EMMPRIN), has been localized to the surface of tumor cells and is implicated in stimulating several matrix metalloproteinases in the fibroblasts. Based upon sequence similarity, yc24_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yc24_(—)1 protein sequence near the N-terminus of SEQ ID NO:24.

Clone “yc25_(—)1”

A polynucleotide of the present invention has been identified as clone “yc25_(—)1”. yc25_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc25_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc25_(—)1 protein”).

The nucleotide sequence of yc25_(—)1 as presently determined is reported in SEQ ID NO:25, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc25_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:26. Amino acids 6 to 18 of SEQ ID NO:26 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 19. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc25_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc25_(—)1 should be approximately 1800 bp.

The nucleotide sequence disclosed herein for yc25_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc25_(—)1 demonstrated at least some similarity with sequences identified as AA332406 (EST36341 Embryo, 8 week I Homo sapiens cDNA 5′ end), T20094 (Human gene signature HUMGS01237), and W73912 (zd71a11.s1 Soares fetal heart NbHH19W Homo sapiens cDNA clone 346076 3′). Based upon sequence similarity, yc25_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “ye2_(—)1”

A polynucleotide of the present invention has been identified as clone “ye2_(—)1”. ye2_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye2_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye2_(—)1 protein”).

The nucleotide sequence of ye2_(—)1 as presently determined is reported in SEQ ID NO:27, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye2_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:28. Amino acids 30 to 42 of SEQ ID NO:28 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 43. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ye2_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ye2_(—)1 should be approximately 1500 bp.

The nucleotide sequence disclosed herein for ye2_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ye2_(—)1 demonstrated at least some similarity with sequences identified as AA354797 (EST63132 Jurkat T-cells V Homo sapiens cDNA 5′ end) and Z43858 (H. sapiens partial cDNA sequence; clone c-1md12). Based upon sequence similarity, ye2_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the ye2_(—)1 protein sequence centered around amino acid 70 of SEQ ID NO:28.

Clone “ya65_(—)1”

A polynucleotide of the present invention has been identified as clone “ya65_(—)1”. ya65_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya65_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya65_(—)1 protein”).

The nucleotide sequence of ya65_(—)1 as presently determined is reported in SEQ ID NO:29, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya65_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:30.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya65_(—)1 should be approximately 550 bp.

The nucleotide sequence disclosed herein for ya65_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya65_(—)1 demonstrated at least some similarity with sequences identified as AI005084 (ou08g10.x1 Soares_NFL_T_GBC_S1 Homo sapiens cDNA clone IMAGE:1625730 3′, mRNA sequence). Based upon sequence similarity, ya65_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the ya65_(—)1 protein sequence centered around amino acid 87 of SEQ ID NO:30.

Clone “yb60_(—)1”

A polynucleotide of the present invention has been identified as clone “yb60_(—)1”. yb60_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb60_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb60_(—)1 protein”).

The nucleotide sequence of yb60_(—)1 as presently determined is reported in SEQ ID NO:31, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb60_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:32. Amino acids 46 to 58 of SEQ ID NO:32 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 59. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb60_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb60_(—)1 should be approximately 2500 bp.

The nucleotide sequence disclosed herein for yb60_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb60_(—)1 demonstrated at least some similarity with sequences identified as AA505869 (nh99f02.s1 NCI_CGAP_Br2 Homo sapiens cDNA clone IMAGE:966651), H29487 (ym60a10.r1 Homo sapiens cDNA clone 52621 5′), and T24510 (Human gene signature HUMGS06552; standard; cDNA to mRNA). Based upon sequence similarity, yb60_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yb139_(—)1”

A polynucleotide of the present invention has been identified as clone “yb139_(—)1”. yb139_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb139_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb139_(—)1 protein”).

The nucleotide sequence of yb139_(—)1 as presently determined is reported in SEQ ID NO:33, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb139_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:34. Amino acids 101 to 113 of SEQ ID NO:34 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 114. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb139_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb139_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yb139_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb139_(—)1 demonstrated at least some similarity with sequences identified as AA332206 (EST36115 Embryo, 8 week I Homo sapiens cDNA 5′ end, mRNA sequence). Based upon sequence similarity, yb139_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yb139_(—)1 protein sequence centered around amino acid 42 of SEQ ID NO:34. The nucleotide acid sequence of yb139_(—)1 indicates that it may contain sequences similar to a primate simple repeat and to the M. serrator retropseudogene-like repetitive element I.

Clone “yc29_(—)1”

A polynucleotide of the present invention has been identified as clone “yc29_(—)1”. yc29_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc29_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc29_(—)1 protein”).

The nucleotide sequence of yc29_(—)1 as presently determined is reported in SEQ ID NO:35, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc29_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:36.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc29_(—)1 should be approximately 2100 bp.

The nucleotide sequence disclosed herein for yc29_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc29_(—)1 demonstrated at least some similarity with sequences identified as AA195033 (zr35a12.s1 Soares NhHMPu S1 Homo sapiens cDNA clone 665374 3′, mRNA sequence), AF046001 (Homo sapiens zinc finger transcription factor (ZNF207) mRNA, complete cds), and T23300 (Human gene signature HUMGS05114; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yc29_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yc29_(—)1 protein demonstrated at least some similarity to the sequence identified as AF046001 (zinc finger transcription factor [Homo sapiens]). The presence of zinc fingers in a protein may indicate that the protein has a DNA-binding function, but zinc fingers may also be protein-protein interaction domains.

Based upon sequence similarity, yc29_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yc29_(—)1 protein sequence, one centered around amino acid 175 and another around amino acid 210 of SEQ ID NO:36.

yc29_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 56 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yc40_(—)1”

A polynucleotide of the present invention has been identified as clone “yc40_(—)1”. yc40_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc40_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc40_(—)1 protein”).

The nucleotide sequence of yc40_(—)1 as presently determined is reported in SEQ ID NO:37, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc40_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:38. Amino acids 31 to 43 of SEQ ID NO:38 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 44. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc40_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc40_(—)1 should be approximately 1400 bp.

The nucleotide sequence disclosed herein for yc40_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc40_(—)1 demonstrated at least some similarity with sequences identified as D62445 (Human aorta cDNA 5′-end GEN-286A10, mRNA sequence) and T25162 (Human gene signature HUMGS07322; standard; DNA). Based upon sequence similarity, yc40_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yc40_(—)1 protein sequence centered around amino acid 50 of SEQ ID NO:38.

Clone “yd10_(—)1”

A polynucleotide of the present invention has been identified as clone “yd10_(—)1”. yd10_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd10_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd10_(—)1 protein”).

The nucleotide sequence of yd10_(—)1 as presently determined is reported in SEQ ID NO:39, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd10_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:40. Amino acids 47 to 59 of SEQ ID NO:40 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 60. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd10_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd10_(—)1 should be approximately 825 bp.

The nucleotide sequence disclosed herein for yd10_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd10_(—)1 demonstrated at least some similarity with sequences identified as AA587270 (nn70g03.s1 NCI_CGAP_Lar1 Homo sapiens cDNA clone IMAGE:1089268 similar to contains Alu repetitive element;contains element PTR5 repetitive element; mRNA sequence). Based upon sequence similarity, yd10_(—)1 proteins and each similar protein or peptide may share at least some activity. The nucleotide sequence of yd10_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yf5_(—)1”

A polynucleotide of the present invention has been identified as clone “yf5_(—)1”. yf5_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yf5_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yf5_(—)1 protein”).

The nucleotide sequence of yf5_(—)1 as presently determined is reported in SEQ ID NO:41, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yf5_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:42. Amino acids 9 to 21 of SEQ ID NO:42 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 22. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yf5_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yf5_(—)1 should be approximately 1800 bp.

The nucleotide sequence disclosed herein for yf5_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yf5_(—)1 demonstrated at least some similarity with sequences identified as AA181631 (zp52a03.s1 Stratagene HeLa cell s3 937216 Homo sapiens cDNA clone 613036 3′, mRNA sequence) and U49082 (Human transporter protein (g17) mRNA, complete cds). The predicted amino acid sequence disclosed herein for yf5_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yf5_(—)1 protein demonstrated at least some similarity to the sequence identified as U49082 (transporter protein [Homo sapiens]). Based upon sequence similarity, yf5_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts ten additional potential transmembrane domains within the yf5_(—)1 protein sequence, centered around amino acids 36, 84, 130, 154, 213, 249, 292, 330, 353, and 389 of SEQ ID NO:42, respectively. The nucleotide sequence of yf5_(—)1 indicates that it may contain a MIR repeat region.

Clone “ya67_(—)1”

A polynucleotide of the present invention has been identified as clone “ya67_(—)1”. ya67_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya67_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya67_(—)1 protein”).

The nucleotide sequence of ya67_(—)1 as presently determined is reported in SEQ ID NO:43, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya67_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:44. Amino acids 14 to 26 of SEQ ID NO:44 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 27. Amino acids 16 to 28 are also a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 29. Due to the hydrophobic nature of the predicted leader/signal sequences, each is likely to act as a transmembrane domain should it not be separated from the remainder of the ya67_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya67_(—)1 should be approximately 800 bp.

The nucleotide sequence disclosed herein for ya67_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya67_(—)1 demonstrated at least some similarity with sequences identified as AC002042 (*** SEQUENCING IN PROGRESS *** Homo sapiens chromosome 16p11.2 BAC clone CIT987SK-A-180G2; HTGS phase 1, 5 unordered pieces). Based upon sequence similarity, ya67_(—)1 proteins and each similar protein or peptide may share at least some activity. The nucleotide sequence of ya67_(—)1 indicates that it may contain an MIR repeat sequence.

ya67_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 21 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “ya70_(—)1”

A polynucleotide of the present invention has been identified as clone “ya70_(—)1”. ya70_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya70_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya70_(—)1 protein”).

The nucleotide sequence of ya70_(—)1 as presently determined is reported in SEQ ID NO:45, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya70_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:46.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya70_(—)1 should be approximately 1500 bp.

The nucleotide sequence disclosed herein for ya70_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya70_(—)1 demonstrated at least some similarity with sequences identified as AA813657 (ai69c03.s1 Soares testis NHT Homo sapiens cDNA clone 1376068 3′, mRNA sequence) and U84408 (Human IL-1 receptor related protein MyD88 mRNA, complete cds). The predicted amino acid sequence disclosed herein for ya70_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted ya70_(—)1 protein demonstrated at least some similarity to the sequences identified as U84408 (MyD88 [Homo sapiens]). Human MyD88, an IL-6 primary response gene, encodes a protein containing an N-terminal death domain and a C-terminal region that exhibits homology to human IL-1Rp80 and drosophila Toll (IL-1Rp80 and Toll are homologs). Based upon sequence similarity, ya70_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the ya70_(—)1 protein sequence, one centered around amino acid 90 and another around amino acid 175 of SEQ ID NO:46.

Clone “yb51_(—)1”

A polynucleotide of the present invention has been identified as clone “yb51_(—)1”. yb51_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb51_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb51_(—)1 protein”).

The nucleotide sequence of yb51_(—)1 as presently determined is reported in SEQ ID NO:47, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb51_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:48. Amino acids 5 to 17 of SEQ ID NO:48 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 18. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb51_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb51_(—)1 should be approximately 1400 bp.

The nucleotide sequence disclosed herein for yb51_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb51_(—)1 demonstrated at least some similarity with sequences identified as AA058715 (zk70c03.s1 Soares pregnant uterus NbHPU Homo sapiens cDNA clone 488164 3′ similar to contains Alu repetitive element; contains element MER1 repetitive element) and Z44795 (H. sapiens partial cDNA sequence; clone c-29d08). Based upon sequence similarity, yb51_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yb51_(—)1 protein sequence centered around amino acid 59 of SEQ ID NO:48. The nucleotide sequence of yb51_(—)1 indicates that it may contain at least one repetitive element.

Clone “yb101_(—)1”

A polynucleotide of the present invention has been identified as clone “yb101_(—)1”. yb101_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb101_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb101_(—)1 protein”).

The nucleotide sequence of yb101_(—)1 as presently determined is reported in SEQ ID NO:49, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb101_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:50.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb101_(—)1 should be approximately 1050 bp.

The nucleotide sequence disclosed herein for yb101_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb101_(—)1 demonstrated at least some similarity with sequences identified as AC005060 (Homo sapiens clone RG086D03; HTGS phase 1, 3 unordered pieces) and D60925 (Human fetal brain cDNA 5′-end GEN-139D01, mRNA sequence). Based upon sequence similarity, yb1011 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yb101_(—)1 protein sequence centered around amino acid 11 of SEQ ID NO:50.

yb11_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 8 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yb124_(—)1”

A polynucleotide of the present invention has been identified as clone “yb124_(—)1”. yb124_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb124_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb124_(—)1 protein”).

The nucleotide sequence of yb124_(—)1 as presently determined is reported in SEQ ID NO:51, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb124_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:52.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb124_(—)1 should be approximately 1700 bp.

The nucleotide sequence disclosed herein for yb124_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb124_(—)1 demonstrated at least some similarity with sequences identified as AA430306 (zw68g03.r1 Soares testis NHT Homo sapiens cDNA clone 781396 5′, mRNA sequence). Based upon sequence similarity, yb124_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts three potential transmembrane domains within the yb124_(—)1 protein sequence, centered around amino acids 30, 84, and 134 of SEQ ID NO:52, respectively. Amino acids 128 to 140 of SEQ ID NO:52 also have characteristics indicative of a leader/signal sequence.

Clone “yb125_(—)1”

A polynucleotide of the present invention has been identified as clone “yb125_(—)1”. yb125_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb125_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb125_(—)1 protein”).

The nucleotide sequence of yb125_(—)1 as presently determined is reported in SEQ ID NO:53, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb125_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:54. Amino acids 15 to 27 of SEQ ID NO:54 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 28. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb125_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb125_(—)1 should be approximately 2000 bp.

The nucleotide sequence disclosed herein for yb125_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb125_(—)1 demonstrated at least some similarity with sequences identified as AA340207 (EST45465 Fetal brain m Homo sapiens cDNA 5′ end, mRNA sequence) and Q92781 (Human thymopoietin gene fragment; standard; DNA). Based upon sequence similarity, yb125_(—)1 proteins and each similar protein or peptide may share at least some activity. The nucleotide sequence of yb125_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yb179_(—)1”

A polynucleotide of the present invention has been identified as clone “yb179_(—)1”. yb179_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb179_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb179_(—)1 protein”).

The nucleotide sequence of yb179_(—)1 as presently determined is reported in SEQ ID NO:55, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb179_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:56.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb179_(—)1 should be approximately 1500 bp.

The nucleotide sequence disclosed herein for yb179_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb179_(—)1 demonstrated at least some similarity with sequences identified as AA398428 (zt62a1.s1 Soares testis NHT Homo sapiens cDNA clone 726908 3′, mRNA sequence). Based upon sequence similarity, yb179_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yb179_(—)1 protein sequence centered around amino acid 100 of SEQ ID NO:56. Amino acids 97 to 109 of SEQ ID NO:56 are also a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 110.

Clone “yc48_(—)1”

A polynucleotide of the present invention has been identified as clone “yc48_(—)1”. yc48_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc48_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc48_(—)1 protein”).

The nucleotide sequence of yc48_(—)1 as presently determined is reported in SEQ ID NO:57, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc48_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:58. Amino acids 5 to 17 of SEQ ID NO:58 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 18. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc48_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc48_(—)1 should be approximately 1400 bp.

The nucleotide sequence disclosed herein for yc48_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc48_(—)1 demonstrated at least some similarity with sequences identified as AI009170 (EST203621 Normalized rat embryo, Bento Soares Rattus sp. cDNA clone REMBJ87 3′ end, mRNA sequence). Based upon sequence similarity, yc48_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yc48_(—)1 protein sequence, one centered around amino acid 110 and another around amino acid 180 of SEQ ID NO:58.

Clone “ye21_(—)1”

A polynucleotide of the present invention has been identified as clone “ye21_(—)1”. ye21_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye21_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye21_(—)1 protein”).

The nucleotide sequence of ye21_(—)1 as presently determined is reported in SEQ ID NO:59, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye21_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:60. Amino acids 9 to 21 of SEQ ID NO:60 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 22. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ye21_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ye21_(—)1 should be approximately 1550 bp.

The nucleotide sequence disclosed herein for ye21_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the databases. The TopPredII computer program predicts a potential transmembrane domain within the ye21_(—)1 protein sequence centered around amino acid 66 of SEQ ID NO:60. The nucleotide sequence of ye21_(—)1 indicates that it may contain an Alu repetitive element.

Clone “ye22_(—)1”

A polynucleotide of the present invention has been identified as clone “ye22_(—)1”. ye22_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye22_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye22_(—)1 protein”).

The nucleotide sequence of ye22_(—)1 as presently determined is reported in SEQ ID NO:61, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye22_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:62.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ye22_(—)1 should be approximately 1600 bp.

The nucleotide sequence disclosed herein for ye22_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ye22_(—)1 demonstrated at least some similarity with sequences identified as AJ002553 (*** SEQUENCING IN PROGRESS *** Homo sapiens genomic DNA (PAC 1118i22) from chromosome 11; HTGS phase 1) and T19813 (Human gene signature HUMGS00891; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for ye22_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted ye22_(—)1 protein demonstrated at least some similarity to the sequence identified as AF003145 (No definition line found [Caenorhabditis elegans]). Based upon sequence similarity, ye22_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the ye22_(—)1 protein sequence centered around amino acid 77 of SEQ ID NO:62. The nucleotide sequence of ye22_(—)1 indicates that it may contain repetitive elements.

Clone “ye39_(—)1”

A polynucleotide of the present invention has been identified as clone “ye39_(—)1”. ye39_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye39_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye39_(—)1 protein”).

The nucleotide sequence of ye39_(—)1 as presently determined is reported in SEQ ID NO:63, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye39_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:64.

The EcoRI/NotI restriction fragment obtainable from the deposit containing done ye39_(—)1 should be approximately 1700 bp.

The nucleotide sequence disclosed herein for ye39_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ye39_(—)1 demonstrated at least some similarity with sequences identified as AA360300 (EST69467 Liver II Homo sapiens cDNA 5′ end, mRNA sequence). Based upon sequence similarity, ye39_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the ye39_(—)1 protein sequence, one centered around amino acid 20 and another around amino acid 45 of SEQ ID NO:64.

Clone “yf9_(—)1”

A polynucleotide of the present invention has been identified as clone “yf9_(—)1”. yf9_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yf9_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yf9_(—)1 protein”).

The nucleotide sequence of yf9_(—)1 as presently determined is reported in SEQ ID NO:65. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yf9_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:66.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yf9_(—)1 should be approximately 950 bp.

The nucleotide sequence disclosed herein for yf9_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yf9_(—)1 demonstrated at least some similarity with sequences identified as AA747796 (nx86a03.s1 NCI_CGAP_GCB1 Homo sapiens cDNA clone IMAGE 1269100, mRNA sequence) and AF009426 (Homo sapiens clone 22 mRNA, alternative splice variant beta-1, complete cds). The predicted amino acid sequence disclosed herein for yf9_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yf9_(—)1 protein demonstrated at least some similarity to the sequence identified as AF009426 (clone 22 [Homo sapiens]). Based upon sequence similarity, yf9_(—)1 proteins and each similar protein or peptide may share at least some activity. Clone 22 mRNA was identified from brain transcripts and the corresponding gene has been localized to chromosome 18; the chromosome regions 18p and 18q where the transcripts cluster are candidate regions for bipolar disorder. The protein products of the clone 22 mRNA variants are predicted to be membrane spanning. (Yoshikawa et al., 1997, Am. J. Med. Genet. 74(2): 140-149, which is incorporated by reference herein). The predicted yf9_(—)1 protein appears to be a novel splice variant expressed from the clone 22 gene. The TopPredII computer program predicts a potential transmembrane domain within the yf9_(—)1 protein sequence centered around amino acid 39 of SEQ ID NO:66.

yf9_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 24 kDa was detected in conditioned medium and membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yh4_(—)1”

A polynucleotide of the present invention has been identified as clone “yh4_(—)1”. yh4_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh4_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh4_(—)1 protein”).

The nucleotide sequence of yh4_(—)1 as presently determined is reported in SEQ ID NO:67, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh4_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:68.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh4_(—)1 should be approximately 1500 bp.

The nucleotide sequence disclosed herein for yh4_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the databases. The TopPredII computer program predicts a potential transmembrane domain within the yh4_(—)1 protein sequence centered around amino acid 80 of SEQ ID NO:68. The nucleotide sequence of yh4_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yi4_(—)1”

A polynucleotide of the present invention has been identified as clone “yi4_(—)1”. yi4_(—)1 was isolated from a human brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi4_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi4_(—)1 protein”).

The nucleotide sequence of yi4_(—)1 as presently determined is reported in SEQ ID NO:69, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yi4_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:70. Amino acids 18 to 30 of SEQ ID NO:70 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 31. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi4_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi4_(—)1 should be approximately 1400 bp.

The nucleotide sequence disclosed herein for yi4_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi4_(—)1 demonstrated at least some similarity with sequences identified as AA553835 (nk94f03.s1 NCI_CGAP_Co11 Homo sapiens cDNA clone IMAGE:1028477, mRNA sequence) and T22931 (Human gene signature HUMGS04656; standard; cDNA to mRNA). Based upon sequence similarity, yi4_(—)1 proteins and each similar protein or peptide may share at least some activity. The nucleotide sequence of yi4_(—)1 indicates that it may contain simple nucleotide repeat sequences.

Clone “yj3_(—)1”

A polynucleotide of the present invention has been identified as clone “yj3_(—)1”. yj3_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj3_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj3_(—)1 protein”).

The nucleotide sequence of yj3_(—)1 as presently determined is reported in SEQ ID NO:71, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj3_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:72. Amino acids 8 to 20 of SEQ ID NO:72 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 21. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yj3_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yj3_(—)1 should be approximately 900 bp.

The nucleotide sequence disclosed herein for yj3_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yj3_(—)1 demonstrated at least some similarity with sequences identified as AC004955 (Homo sapiens clone DJ1087M19; HTGS phase 1, 7 unordered pieces) and W37665 (zc12f05.r1 Soares parathyroid tumor NbHPA Homo sapiens cDNA clone 322113 5′, mRNA sequence). Based upon sequence similarity, yj3_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts four additional potential transmembrane domains within the yj3_(—)1 protein sequence, centered around amino acids 17, 45, 87, and 110 of SEQ ID NO:72, respectively.

Clone “yj7_(—)1”

A polynucleotide of the present invention has been identified as clone “yj7_(—)1”. yj7_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj7_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj7_(—)1 protein”).

The nucleotide sequence of yj7_(—)1 as presently determined is reported in SEQ ID NO:73, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj7_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:74. Amino acids 21 to 33 of SEQ ID NO:74 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 34. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yj7_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yj7_(—)1 should be approximately 1159 bp.

The nucleotide sequence disclosed herein for yj7_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yj7_(—)1 demonstrated at least some similarity with sequences identified as AA827998 (of10c11.s1 NCI_CGAP_Co12 Homo sapiens cDNA clone IMAGE:1420724 3′, mRNA sequence), C80074 (Mus musculus 3.5-dpc blastocyst cDNA 3′-end sequence, mRNA sequence), and T25792 (Human gene signature HUMGS08020; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yj7_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yj7_(—)1 protein demonstrated at least some similarity to sequences identified as R61477 (Clavulanic acid dehydrogenase sequence), U43283 (similar to the insect-type alcohol dehydrogenase/ribitol dehydrogenase family [Caenorhabditis elegans]), and Z99116 (similar to ketoacyl reductase [Bacillus subtilus]).

Based upon sequence similarity, yj7_(—)1 proteins and each similar protein or peptide may share at least some activity. Motifs search revealed the short-chain alcohol dehydrogenase family signature. These dehydrogenases and reductases are cytoplasmic, however, the amino acid similarity alignment is more consistent with domain/motif sharing. Also, the predicted yj7_(—)1 protein demonstrates similarity to proteins that are only “similar to” these dehydrogenase and reductase enzymes; the predicted yj7_(—)1 protein exhibits less amino acid similarity to the enzymes themselves. Therefore,the predicted yj7_(—)1 protein might be a novel, secreted form of alcohol dehydrogenase.

yj7_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 32 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yj10_(—)1”

A polynucleotide of the present invention has been identified as clone “yj10_(—)1”. yj10_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj10_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj10_(—)1 protein”).

The nucleotide sequence of yj10_(—)1 as presently determined is reported in SEQ ID NO:75, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj10_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:76.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yj10_(—)1 should be approximately 1600 bp.

The nucleotide sequence disclosed herein for yj10_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yj10_(—)1 demonstrated at least some similarity with sequences identified as AF072860 (Homo sapiens protein activator of the interferon-induced protein kinase (PACT) mRNA, complete cds), AI056368 (oy48c07.x1 NCI_CGAP_Brn23 Homo sapiens cDNA clone IMAGE 1669068 3′ similar to TR Q91836 Q91836 RNA BINDING PROTEIN; mRNA sequence) and T24520 (Human gene signature HUMGS06564; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yj10_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yj10_(—)1 protein demonstrated at least some similarity to the sequence identified as AF072860 (protein activator of the interferon-induced protein kinase [Homo sapiens]). Based upon sequence similarity, yj10_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yj28_(—)1”

A polynucleotide of the present invention has been identified as clone “yj28_(—)1”. yj28_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj28_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj28_(—)1 protein”).

The nucleotide sequence of yj28_(—)1 as presently determined is reported in SEQ ID NO:77, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj28_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:78. Amino acids 160 to 172 of SEQ ID NO:78 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 173. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yj28_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing done yj28_(—)1 should be approximately 1250 bp.

The nucleotide sequence disclosed herein for yj28_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yj28_(—)1 demonstrated at least some similarity with sequences identified as AA402090 (zu53f03.r1 Soares ovary tumor NbHOT Homo sapiens cDNA clone 741725 5′, mRNA sequence) and AJ009691 (Podocoryne carnea mRNA for SMC2orf protein, partial). The predicted amino acid sequence disclosed herein for yj28_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yj28_(—)1 protein demonstrated at least some similarity to the sequence identified as AJ009691 (SMC2orf [Podocoryne carnea]). Based upon sequence similarity, yj28_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yj28_(—)1 protein sequence centered around amino acid 348 of SEQ ID NO:78.

Clone “yj29_(—)1”

A polynucleotide of the present invention has been identified as clone “yj29_(—)1”. yj29_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj29_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj29_(—)1 protein”).

The nucleotide sequence of yj29_(—)1 as presently determined is reported in SEQ ID NO:79, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj29_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:80. Amino acids 310 to 322 of SEQ ID NO:80 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 323. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yj29_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yj29_(—)1 should be approximately 1600 bp.

The nucleotide sequence disclosed herein for yj29_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yj29_(—)1 demonstrated at least some similarity with sequences identified as AA156900 (zl20c06.r1 Soares pregnant uterus NbHPU Homo sapiens cDNA clone 502474 5′ similar to WP:T06D8.8 CE02329; mRNA sequence), AF015416 (Homo sapiens chromosome 11 from 11p15.5 region, complete sequence), and T23342 Human gene signature HUMGS05162; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yj29_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yj29_(—)1 protein demonstrated at least some similarity to the sequence identified as Z49130 (T06D8.8 [Caenorhabditis elegans]). Based upon sequence similarity, yj29_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yj29_(—)1 protein sequence centered around amino acid 207 of SEQ ID NO:80.

Clone “yj32_(—)1”

A polynucleotide of the present invention has been identified as clone “yj32_(—)1”. yj32_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj32_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj32_(—)1 protein”).

The nucleotide sequence of yj32_(—)1 as presently determined is reported in SEQ ID NO:81, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj32_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:82. Amino acids 64 to 76 of SEQ ID NO:82 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 77. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yj32_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yj32_(—)1 should be approximately 1450 bp.

The nucleotide sequence disclosed herein for yj32_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the databases. The TopPredII computer program predicts an additional potential transmembrane domain within the yj32_(—)1 protein sequence, near the N-terminus of SEQ ID NO:82. The nucleotide sequence of yj32_(—)1 indicates that it may contain an Alu repetitive element. yj32_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 10 kDa was detected in conditioned medium using SDS polyacrylamide gel electrophoresis.

Clone “yb186_(—)1”

A polynucleotide of the present invention has been identified as clone “yb186_(—)1”. yb186_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb186_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb186_(—)1 protein”).

The nucleotide sequence of yb186_(—)1 as presently determined is reported in SEQ ID NO:83, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb186_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:84. Amino acids 10 to 22 of SEQ ID NO:84 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 23. Amino acids 14 to 26 of SEQ ID NO:84 are also a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning in this case at amino acid 27. Due to the hydrophobic nature of the predicted leader/signal sequences, each is likely to act as a transmembrane domain should it not be separated from the remainder of the yb186_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb186_(—)1 should be approximately 2700 bp.

The nucleotide sequence disclosed herein for yb186_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb186_(—)1 demonstrated at least some similarity with sequences identified as T25270 (Human gene signature HUMGS07432; standard; cDNA to mRNA) and W73738 (zd50d05.s1 Soares fetal heart NbHH19W Homo sapiens cDNA clone 344073 3′, mRNA sequence). Based upon sequence similarity, yb186_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yb186_(—)1 protein sequence centered around amino acid 243 of SEQ ID NO:84.

Clone “yb226_(—)1”

A polynucleotide of the present invention has been identified as clone “yb226_(—)1”. yb226_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb226_(—)1 is a full-length done, including the entire coding sequence of a secreted protein (also referred to herein as “yb226_(—)1 protein”).

The nucleotide sequence of yb226_(—)1 as presently determined is reported in SEQ ID NO:85, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb226_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:86.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb226_(—)1 should be approximately 1800 bp.

The nucleotide sequence disclosed herein for yb226_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb226_(—)1 demonstrated at least some similarity with sequences identified as N72056 (yv29f11.r1 Soares fetal liver spleen 1NFLS Homo sapiens cDNA clone 244173 5′, mRNA sequence). Based upon sequence similarity, yb226_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yb226_(—)1 protein sequence, one around amino acid 54 and another around amino acid 122 of SEQ ID NO:86. Amino acids 45 to 57 and 77 to 89 of SEQ ID NO:86 are also possible leader/signal sequences, with the predicted mature amino acid sequences beginning at amino acids 58 and 90, respectively.

Clone “yd50_(—)1”

A polynucleotide of the present invention has been identified as clone “yd50_(—)1”. yd50_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd50_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd50_(—)1 protein”).

The nucleotide sequence of yd50_(—)1 as presently determined is reported in SEQ ID NO:87, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd50_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:88.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd50_(—)1 should be approximately 900 bp.

The nucleotide sequence disclosed herein for yd50_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd50_(—)1 demonstrated at least some similarity with sequences identified as AA037761 (zk38c07.s1 Soares pregnant uterus NbHPU Homo sapiens cDNA clone 485100 3′, mRNA sequence), AA312218 (EST182969 Jurkat T-cells VI Homo sapiens cDNA 5′ end, mRNA sequence), and T24178 (Human gene signature HUMGS06183; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yd50_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd50_(—)1 protein demonstrated at least some similarity to sequences identified as AF038613 (undefined protein [Caenorhabditis elegans]) and AL023286 (hypothetical protein [Schizosaccharomyces pombe]). Based upon sequence similarity, yd50_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yd50_(—)1 protein sequence centered around amino acid 45 of SEQ ID NO:88.

Clone “yd51_(—)1”

A polynucleotide of the present invention has been identified as clone “yd51_(—)1”. yd51_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd51_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd51_(—)1 protein”).

The nucleotide sequence of yd51_(—)1 as presently determined is reported in SEQ ID NO:89, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd51_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:90. Amino acids 11 to 23 of SEQ ID NO:90 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 24. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd51_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd51_(—)1 should be approximately 800 bp.

The nucleotide sequence disclosed herein for yd51_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd51_(—)1 demonstrated at least some similarity with sequences identified as AA205661 (zq68g09.s1 Stratagene neuroepithelium (#937231) Homo sapiens cDNA clone 646816 3′, mRNA sequence). Based upon sequence similarity, yd51_(—)1 proteins and each similar protein or peptide may share at least some activity.

yd51_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 24 kDa was detected in conditioned medium and membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yd73_(—)1”

A polynucleotide of the present invention has been identified as clone “yd73_(—)1”. yd73_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd73_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd73_(—)1 protein”).

The nucleotide sequence of yd73_(—)1 as presently determined is reported in SEQ ID NO:91, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd73_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:92. Amino acids 67 to 79 of SEQ ID NO:92 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 80. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd73_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd73_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yd73_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd73_(—)1 demonstrated at least some similarity with sequences identified as AA587100 (nn81g06.s1 NCI_CGAP_Co9 Homo sapiens cDNA clone IMAGE:1090330, mRNA sequence) and T51192 (Human breast specific gene BSG10 partial cDNA clone HBGDM44; standard; cDNA). The predicted amino acid sequence disclosed herein for yd73_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd73_(—)1 protein demonstrated at least some similarity to the sequence identified as AF000198 (No definition line found (T28F2.2) [Caenorhabditis elegans]). Based upon sequence similarity, yd73_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yd73_(—)1 protein sequence, one centered around amino acid 74 and another around amino acid 169 of SEQ ID NO:92.

yd73_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “ye43_(—)1”

A polynucleotide of the present invention has been identified as clone “ye43_(—)1”. ye43_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye43_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye43_(—)1 protein”).

The nucleotide sequence of ye43_(—)1 as presently determined is reported in SEQ ID NO:93, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye43_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:94. Amino acids 88 to 100 of SEQ ID NO:94 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 101. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ye43_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ye43_(—)1 should be approximately 1500 bp.

The nucleotide sequence disclosed herein for ye43_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ye43_(—)1 demonstrated at least some similarity with sequences identified as T23444 (Human gene signature HUMGS05282; standard; cDNA to mRNA) and Z99353 (Homo sapiens mRNA; expressed sequence tag; clone DKFZphamy1_(—)1a12, 3′ read, mRNA sequence). Based upon sequence similarity, ye43_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the ye43_(—)1 protein sequence, one centered around amino acid 51 and another around amino acid 89 of SEQ ID NO:94.

Clone “yh71_(—)1”

A polynucleotide of the present invention has been identified as clone “yh71_(—)1”. yh71_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh71_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh71_(—)1 protein”).

The nucleotide sequence of yh71_(—)1 as presently determined is reported in SEQ ID NO:95, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh71_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:96. Amino acids 264 to 276 of SEQ ID NO:96 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 277. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yh71_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh71_(—)1 should be approximately 1891 bp.

The nucleotide sequence disclosed herein for yh71_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yh71_(—)1 demonstrated at least some similarity with sequences identified as H10493 (yl90h09.r1 Homo sapiens cDNA clone 45675 5′), T39809 (Mouse H74 gene; standard; DNA), and X85124 (M.musculus pacsin gene). Based upon sequence similarity, yh71_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yh71_(—)1 protein sequence, one centered around amino acid 122 and another around amino acid 190 of SEQ ID NO:96.

Clone “yh100_(—)1”

A polynucleotide of the present invention has been identified as clone “yh100_(—)1”. yh100_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh100_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh100_(—)1 protein”).

The nucleotide sequence of yh100_(—)1 as presently determined is reported in SEQ ID NO:97, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh100_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:98. Amino acids 35 to 47 of SEQ ID NO:98 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino add 48. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yh100_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh100_(—)1 should be approximately 2200 bp.

The nucleotide sequence disclosed herein for yh100_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts an additional potential transmembrane domain within the yh100_(—)1 protein sequence, around amino acid 73 of SEQ ID NO:98. The nucleotide sequence of yh100_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yi3_(—)1”

A polynucleotide of the present invention has been identified as clone “yi3_(—)1”. yi3_(—)1 was isolated from a human brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi3_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi3_(—)1 protein”).

The nucleotide sequence of yi3_(—)1 as presently determined is reported in SEQ ID NO:99, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yi3_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:100. Amino acids 20 to 32 of SEQ ID NO:100 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 33. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi3_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi3_(—)1 should be approximately 2000 bp.

The nucleotide sequence disclosed herein for yi3_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi3_(—)1 demonstrated at least some similarity with sequences identified as N22677 (yx64a05.s1 Homo sapiens cDNA clone 266480 3′). Based upon sequence similarity, yi3_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yj23_(—)1”

A polynucleotide of the present invention has been identified as clone “yj23_(—)1”. yj23_(—)1 was isolated from a human fetal kidney (293 cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yj23_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yj23_(—)1 protein”).

The nucleotide sequence of yj23_(—)1 as presently determined is reported in SEQ ID NO:101, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yj23_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:102. Amino acids 12 to 24 of SEQ ID NO:102 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 25. Amino acids 15 to 27 of SEQ ID NO:102 are also a possible leader/signal sequence, with the predicted mature amino acid sequence beginning in this case at amino acid 28, or are a transmembrane domain. Due to the hydrophobic nature of the predicted leader/signal sequences, each is likely to act as a transmembrane domain should it not be separated from the remainder of the yj23_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yj23_(—)1 should be approximately 1400 bp.

The nucleotide sequence disclosed herein for yj23_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yj23_(—)1 demonstrated at least some similarity with sequences identified as A1096483 (qa03c12.x1 NCI_CGAP_Brn23 Homo sapiens cDNA clone IMAGE:1685686 3′ similar to TR:Q04386 Q04386 HYPOTHETICAL 29.1 KD PROTEIN IN RPII140 5′ REGION; mRNA sequence) and T19036 (Human gene signature HUMGS00043; standard; cDNA to mRNA). Based upon sequence similarity, yj23_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yj23_(—)1 protein sequence, one centered around amino acid 90 and another around amino acid 199 of SEQ ID NO:102.

Clone “yl9_(—)1”

A polynucleotide of the present invention has been identified as clone “yl9_(—)1”. yl9_(—)1 was isolated from a human adult spleen cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yl9_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yl9_(—)1 protein”).

The nucleotide sequence of yl9_(—)1 as presently determined is reported in SEQ ID NO:103, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yl9_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:104. Amino acids 6 to 18 of SEQ ID NO:104 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 19. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yl9_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yl9_(—)1 should be approximately 1100 bp.

The nucleotide sequence disclosed herein for yl9_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yl9_(—)1 demonstrated at least some similarity with sequences identified as AA902287 (ok69g10.s1 NCI_CGAP_GC4 Homo sapiens cDNA clone IMAGE 1519266 3′ similar to SW C1QA_HUMAN P02745 COMPLEMENT C1Q SUBCOMPONENT, A CHAIN PRECURSOR; mRNA sequence) and X58861 (Mouse mRNA for complement subcomponent C1Q alpha-chain). The predicted amino acid sequence disclosed herein for yl9_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yl9_(—)1 protein demonstrated at least some similarity to sequences identified as R22265 (New collagen type protein from chipmunk blood), W09108 (Human adipocyte complement related protein Acrp30), and X58861 (complement subcomponent C1Q A-chain precursor [Mus musculus]). Based upon sequence similarity, yl9_(—)1 proteins and each similar protein or peptide may share at least some activity. The predicted yl9_(—)1 protein has at least some similarity to human, mouse, and rat complement subcomponent C1Q, and motifs and profile hidden markov model analysis of the predicted yl9_(—)1 protein have revealed the presence of a C1Q domain signature at amino acids 116 to 241 of SEQ ID NO:104. C1Q is a subunit of the C1 enzyme complex that activates the serum complement system. The collagen-like regions of C1Q interact with the Ca(2+)-Dependent C1R(2)/C1S(2) proenzyme complex, and efficient activation of C1 takes place on interaction of the globular heads of C1Q with the Fc regions of IgG or IgM antibody present in immune complexes. The C1Q domain has been found in the C-terminus of vertebrate secreted or membrane-bound proteins which are mostly short-chain collagens and collagen-like molecules. The predicted yl9_(—)1 protein appears to encode a novel member of the C1 enzyme complex, having the highest degree of similarity to the A-chain of the complex. The TopPredII computer program predicts a potential transmembrane domain within the yl9_(—)1 protein sequence centered around amino acid 160 of SEQ ID NO:104.

yl9_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “ya66_(—)1”

A polynucleotide of the present invention has been identified as clone “ya66_(—)1”. ya66_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya66_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya66_(—)1 protein”).

The nucleotide sequence of ya66_(—)1 as presently determined is reported in SEQ ID NO:105, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya66_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:106.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya66_(—)1 should be approximately 1050 bp.

The nucleotide sequence disclosed herein for ya66_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya66_(—)1 demonstrated at least some similarity with sequences identified as AI096636 (qb57c12.x1 NCI_CGAP_Brn23 Homo sapiens cDNA clone IMAGE:1704214 3′, mRNA sequence) and T20099 (Human gene signature HUMGS01242; standard; cDNA to mRNA). Based upon sequence similarity, ya66_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the ya66_(—)1 protein sequence centered around amino acid 106 of SEQ ID NO:106.

Clone “yb187_(—)1”

A polynucleotide of the present invention has been identified as clone “yb187_(—)1”. yb187_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb187_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb187_(—)1 protein”).

The nucleotide sequence of yb187_(—)1 as presently determined is reported in SEQ ID NO:107, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb187_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:108.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb187_(—)1 should be approximately 1800 bp.

The nucleotide sequence disclosed herein for yb187_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb187_(—)1 demonstrated at least some similarity with sequences identified as AA846805 (aj99f04.s1 Soares parathyroid tumor NbHPA Homo sapiens cDNA clone IMAGE:1404607 3′, mRNA sequence) and Q61039 (Human brain Expressed Sequence Tag EST01102; standard; DNA). Based upon sequence similarity, yb187_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yb187_(—)1 protein sequence centered around amino acid 58 of SEQ ID NO:108; amino acids 58 to 70 of SEQ ID NO:108 are also a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 71.

Clone “yb219_(—)1”

A polynucleotide of the present invention has been identified as clone “yb219_(—)1”. yb219_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb219_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb219_(—)1 protein”).

The nucleotide sequence of yb219_(—)1 as presently determined is reported in SEQ ID NO:109, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb219_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:110. Amino acids 3 to 15 of SEQ ID NO:110 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 16. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb219_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb219_(—)1 should be approximately 1600 bp.

The nucleotide sequence disclosed herein for yb219_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database.

Clone “yb228_(—)1”

A polynucleotide of the present invention has been identified as clone “yb228_(—)1”. yb228_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb228_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb228_(—)1 protein”).

The nucleotide sequence of yb228_(—)1 as presently determined is reported in SEQ ID NO:111, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb228_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:112. Amino acids 1 to 13 of SEQ ID NO:112 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 14. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb228_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb228_(—)1 should be approximately 650 bp.

The nucleotide sequence disclosed herein for yb228_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No hits were found in the database. The TopPredII computer program predicts a potential transmembrane domain within the yb228_(—)1 protein sequence centered around amino acid 31 of SEQ ID NO:112.

Clone “yc27_(—)1”

A polynucleotide of the present invention has been identified as clone “yc27_(—)1”. yc27_(—)1 was isolated from a human fetal kidney (293 embryonal carcinoma cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc27_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc27_(—)1 protein”).

The nucleotide sequence of yc27_(—)1 as presently determined is reported in SEQ ID NO:113, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc27_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:114. Amino acids 111 to 123 of SEQ ID NO:114 are a predicted leader/signal sequence, with the predicted mature amino add sequence beginning at amino add 124. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yc27_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc27_(—)1 should be approximately 1300 bp.

The nucleotide sequence disclosed herein for yc27_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc27_(—)1 demonstrated at least some similarity with sequences identified as T23290 (Human gene signature HUMGS05104; standard; cDNA to mRNA) and W60958 (zc98d11.s1 Pancreatic Islet Homo sapiens cDNA clone 339189 3′, mRNA sequence). The predicted amino acid sequence disclosed herein for yc27_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yc27_(—)1 protein demonstrated at least some similarity to sequences identified as AL021890 (undefined protein [Arabidopsis thaliana]) and U00036 (R151.6 [Caenorhabditis elegans]). Based upon sequence similarity, yc27_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts three potential transmembrane domains within the yc27_(—)1 protein sequence, centered around amino acids 68, 107, and 161 of SEQ ID NO:114, respectively.

yc27_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yc49_(—)1”

A polynucleotide of the present invention has been identified as clone “yc49_(—)1”. yc49_(—)1 was isolated from a human fetal kidney (293 embryonal carcinoma cell line) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yc49_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yc49_(—)1 protein”).

The nucleotide sequence of yc49_(—)1 as presently determined is reported in SEQ ID NO:115, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yc49_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:116.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yc49_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yc49_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yc49_(—)1 demonstrated at least some similarity with sequences identified as AF052113 (Homo sapiens clone 23675 mRNA sequence), N28761 (yx69b12.r1 Homo sapiens cDNA clone 266975 5′), and T20571 (Human gene signature HUMGS01786; standard; cDNA to mRNA). Based upon sequence similarity, yc49_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yc49_(—)1 protein sequence, one centered around amino acid 48 and another around amino acid 75 of SEQ ID NO:116. Amino acids 38 to 50 of SEQ ID NO:116 are also a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 51.

Clone “yd40_(—)1”

A polynucleotide of the present invention has been identified as clone “yd40_(—)1”. yd40_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd40_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd40_(—)1 protein”).

The nucleotide sequence of yd40_(—)1 as presently determined is reported in SEQ ID NO:117, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd40_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:118.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd40_(—)1 should be approximately 900 bp.

The nucleotide sequence disclosed herein for yd40_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts three potential transmembrane domains within the yd40_(—)1 protein sequence, centered around amino acids 19, 60, and 86 of SEQ ID NO:118, respectively. The nucleotide sequence of yd40_(—)1 indicates that it may contain a MIR repetitive element.

Clone “yd64_(—)1”

A polynucleotide of the present invention has been identified as clone “yd64_(—)1”. yd64_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd64_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd64_(—)1 protein”).

The nucleotide sequence of yd64_(—)1 as presently determined is reported in SEQ ID NO:119, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd64_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:120.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd64_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yd64_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd64_(—)1 demonstrated at least some similarity with sequences identified as N59133 (yz62c12.s1 Soares multiple sclerosis 2NbHMSP Homo sapiens cDNA clone 287638 3′, mRNA sequence). The predicted amino acid sequence disclosed herein for yd64_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd64_(—)1 protein demonstrated at least some similarity to sequences identified as M98529 (21 kDa protein [Homo sapiens]). Based upon sequence similarity, yd64_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domains within the yd64_(—)1 protein sequence centered around amino acid 96 of SEQ ID NO:120.

yd64_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in conditioned medium using SDS polyacrylamide gel electrophoresis.

Clone “ye47_(—)1”

A polynucleotide of the present invention has been identified as clone “ye47_(—)1”. ye47_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye47_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye471 protein”).

The nucleotide sequence of ye471 as presently determined is reported in SEQ ID NO:121, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye47_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:122. Amino acids 40 to 52 of SEQ ID NO:122 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 53. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ye47_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ye47_(—)1 should be approximately 1600 bp.

The nucleotide sequence disclosed herein for ye47_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ye47_(—)1 demonstrated at least some similarity with sequences identified as AC000105 (*** SEQUENCING IN PROGRESS *** Homo sapiens Chromosome 22q11.2 MDR Region; HTGS phase 2, 6 ordered pieces). Based upon sequence similarity, ye47_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the ye47_(—)1 protein sequence centered around amino acid 42 of SEQ ID NO:122. The nucleotide sequence of ye47_(—)1 indicates that it may contain one or more of the following repetitive elements: Alu, MIR.

ye47_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 24 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yh50_(—)1”

A polynucleotide of the present invention has been identified as clone “yh50_(—)1”. yh50_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh50_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh50_(—)1 protein”).

The nucleotide sequence of yh50_(—)1 as presently determined is reported in SEQ ID NO:123, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh50_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:124. Amino acids 35 to 47 of SEQ ID NO:124 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 48. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yh50_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh50_(—)1 should be approximately 2515 bp.

The nucleotide sequence disclosed herein for yh50_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yh50_(—)1 demonstrated at least some similarity with sequences identified as N49425 (yv21c11.r1 Homo sapiens cDNA clone 243380 5′ similar to contains Alu repetitive element), Q90512 (CEA clone HindIII-Sau3A fragment; standard; DNA), and R98218 (yq75a05.r1 Homo sapiens cDNA clone 201584 5′ similar to contains Alu repetitive element). Based upon sequence similarity, yh50_(—)1 proteins and each similar protein or peptide may share at least some activity. The nucleotide sequence of yh50_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yh53_(—)1”

A polynucleotide of the present invention has been identified as clone “yh53_(—)1”. yh53_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh53_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh53_(—)1 protein”).

The nucleotide sequence of yh53_(—)1 as presently determined is reported in SEQ ID NO:125, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh53_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:126.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh53_(—)1 should be approximately 1763 bp.

The nucleotide sequence disclosed herein for yh53_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yh53_(—)1 demonstrated at least some similarity with sequences identified as T23683 (Human gene signature HUMGS05558; standard; cDNA to mRNA) and W52762 (zd13a08.r1 Soares fetal heart NbHH19W Homo sapiens cDNA clone 340502 5′, mRNA sequence). Based upon sequence similarity, yh53_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yh53_(—)1 protein sequence centered around amino acid 23 of SEQ ID NO:126.

Clone “yh98_(—)1”

A polynucleotide of the present invention has been identified as clone “yh98_(—)1”. yh98_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh98_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh98_(—)1 protein”).

The nucleotide sequence of yh98_(—)1 as presently determined is reported in SEQ ID NO:127, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh98_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:128. Amino acids 24 to 36 of SEQ ID NO:128 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 37. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yh98_(—)1 protein.

Another potential yh98_(—)1 reading frame and predicted amino acid sequence that could be encoded by basepairs 1381 to 1635 of SEQ ID NO:127 is reported in SEQ ID NO:266. Amino acids 64 to 76 of SEQ ID NO:266 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 77. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the protein of SEQ ID NO:266.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh98_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yh98_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yh98_(—)1 demonstrated at least some similarity with sequences identified as AA187630 (zp73e04.s1 Stratagene HeLa cell s3 937216 Homo sapiens cDNA clone 625854 3′, mRNA sequence), AA632023 (np74d10.s1 NCI_CGAP_Br2 Homo sapiens cDNA clone IMAGE:1132051, mRNA sequence), AA837470 (od20e11.s1 NCI_CGAP_GCB1 Homo sapiens cDNA clone IMAGE:1368524, mRNA sequence), AF034176 (Homo sapiens ntcon5 contig mRNA, partial sequence, mRNA sequence), AF052101 (Homo sapiens clone 23872 mRNA sequence), AI092946 (qa81c03.x1 Soares_fetal_heart_NbHH19W Homo sapiens cDNA clone IMAGE:1693156 3′, mRNA sequence), and Q76621 (Human genome fragment (Preferred); standard; DNA). Based upon sequence similarity, yh98_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “ya69_(—)1”

A polynucleotide of the present invention has been identified as clone “ya69_(—)1”. ya69_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya69_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya69_(—)1 protein”).

The nucleotide sequence of ya69_(—)1 as presently determined is reported in SEQ ID NO:129, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya69_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:130. Amino acids 35 to 47 of SEQ ID NO:130 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 48. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya69_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya69_(—)1 should be approximately 2000 bp.

The nucleotide sequence disclosed herein for ya69_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ya69_(—)1 demonstrated at least some similarity with sequences identified as A1075196 (oy96c08.x1 Soares_fetal_liver_spleen_(—)1NFLS_S1 Homo sapiens cDNA clone IMAGE:1673678 3′, mRNA sequence). Based upon sequence similarity, ya69_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the ya69_(—)1 protein sequence, centered around amino acid 40 of SEQ ID NO:130.

Clone “yd107_(—)1”

A polynucleotide of the present invention has been identified as clone “yd107_(—)1”. yd107_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd107_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd107_(—)1 protein”).

The nucleotide sequence of yd107_(—)1 as presently determined is reported in SEQ ID NO:131, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd107_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:132. Amino acids 37 to 49 of SEQ ID NO:132 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 50. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd107_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd107_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yd107_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd107_(—)1 demonstrated at least some similarity with sequences identified as AA910935 (ok85f02.s1 NCI_CGAP_Kid3 Homo sapiens cDNA clone IMAGE:1520763 3′ similar to WP:R05D11.5 CE06240; mRNA sequence) and T26576 (Human gene signature HUMGS08822; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yd107_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd107_(—)1 protein demonstrated at least some similarity to sequences identified as Z75546 (R05D11.5 [Caenorhabditis elegans]). Based upon sequence similarity, yd107_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yd107_(—)1 protein sequence, one centered around amino acid 48 and another around amino acid 121 of SEQ ID NO:132.

Clone “yd145_(—)1”

A polynucleotide of the present invention has been identified as clone “yd145_(—)1”. yd145_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd145_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd145_(—)1 protein”).

The nucleotide sequence of yd145_(—)1 as presently determined is reported in SEQ ID NO:133, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd145_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:134. Amino acids 3 to 15 of SEQ ID NO:134 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 16. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd145_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd145_(—)1 should be approximately 750 bp.

The nucleotide sequence disclosed herein for yd145_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd145_(—)1 demonstrated at least some similarity with sequences identified as AA432034 (zw80e01.r1 Soares testis NHT Homo sapiens cDNA clone 782520 5′, mRNA sequence) and X87489 (H.sapiens genomic DNA (chromosome 3; clone NL1243D)). Based upon sequence similarity, yd145_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yd145_(—)1 protein sequence centered around amino acid 45 of SEQ ID NO:134.

Clone “yh24_(—)1”

A polynucleotide of the present invention has been identified as clone “yh24_(—)1”. yh24_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh24_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh24_(—)1 protein”).

The nucleotide sequence of yh24_(—)1 as presently determined is reported in SEQ ID NO:135, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh24_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:136. Another potential yh24_(—)1 reading frame and predicted amino acid sequence that could be encoded by basepairs 676 to 939 of SEQ ID NO:135 is reported in SEQ ID NO:267.

The EcoRI/NotI restriction fragment obtainable from the deposit containing done yh24_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yh24_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yh24_(—)1 demonstrated at least some similarity with sequences identified as AA129061 (zo11f12.r1 Stratagene neuroepithelium NT2RAMI 937234 Homo sapiens cDNA clone 567407 5′ similar to TR:G439877 G439877 REVERSE TRANSCRIPTASE; mRNA sequence). Based upon sequence similarity, yh24_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yh24_(—)1 protein sequence of SEQ ID NO:136, one centered around amino acid 52 and another near the N-terminus of SEQ ID NO:136, the latter domain also being a possible signal/leader sequence. Analysis of the possible yh24_(—)1 amino acid sequence of SEQ ID NO:267 reveals a binding-protein-dependent transport systems inner membrane component signature. This signature is present in the integral inner-membrane proteins superfamily which translocate substrates across the membrane.

Clone “yi11_(—)1”

A polynucleotide of the present invention has been identified as clone “yi11_(—)1”. yi11_(—)1 was isolated from a human brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi11_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi11_(—)1 protein”).

The nucleotide sequence of yi11_(—)1 as presently determined is reported in SEQ ID NO:137, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino add sequence of the yi11_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:138. Amino acids 128 to 140 of SEQ ID NO:138 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 141. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi11_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi11_(—)1 should be approximately 1550 bp.

The nucleotide sequence disclosed herein for yi11_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi11_(—)1 demonstrated at least some similarity with sequences identified as AA772340 (ai43c02.s1 Soares parathyroid tumor NbHPA Homo sapiens cDNA clone 1359746 3′, mRNA sequence), T26648 (Human gene signature HUMGS08895; standard; cDNA to mRNA), and U48972 (Mus musculus spindlin (Spin) mRNA, complete cds). Based upon sequence similarity, yi11_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts four potential transmembrane domains within the yi11_(—)1 protein sequence, centered around amino acids 20, 45, 90, and 136 of SEQ ID NO:138, respectively, with the most N-terminal domain also being a possible signal/leader sequence.

Clone “yi18_(—)1”

A polynucleotide of the present invention has been identified as clone “yi18_(—)1”. yi18_(—)1 was isolated from a human brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi18_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi18_(—)1 protein”).

The nucleotide sequence of yi18_(—)1 as presently determined is reported in SEQ ID NO:139, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yi18_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:140. Amino acids 48 to 60 of SEQ ID NO:140 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 61. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi18_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi18_(—)1 should be approximately 1850 bp.

The nucleotide sequence disclosed herein for yi18_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi18_(—)1 demonstrated at least some similarity with sequences identified as AC003086 Human BAC clone RG104F04 from 7q21-q22, complete sequence), T81349 (yd27c10.s1 Homo sapiens cDNA clone 109458 3′), and T81524 (yd27c10.r1 Homo sapiens cDNA clone 109458 5′). Based upon sequence similarity, yi18_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yk14_(—)1”

A polynucleotide of the present invention has been identified as clone “yk14_(—)1”. yk14_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk14_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk14_(—)1 protein”).

The nucleotide sequence of yk14_(—)1 as presently determined is reported in SEQ ID NO:141, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk14_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:142. Amino acids 17 to 29 of SEQ ID NO:142 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 30. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk14_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk14_(—)1 should be approximately 1067 bp.

The nucleotide sequence disclosed herein for yk14_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk14_(—)1 demonstrated at least some similarity with sequences identified as AA576618 (nm74f07.s1 NCI_CGAP_Co9 Homo sapiens cDNA clone IMAGE:1073989, mRNA sequence). Based upon sequence similarity, yk14_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domains within the yk14_(—)1 protein sequence centered around amino acid 61 of SEQ ID NO:142.

Clone “yk39_(—)1”

A polynucleotide of the present invention has been identified as clone “yk39_(—)1”. yk39_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk39_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk39_(—)1 protein”).

The nucleotide sequence of yk39_(—)1 as presently determined is reported in SEQ ID NO:143, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk39_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:144.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk39_(—)1 should be approximately 1300 bp.

The nucleotide sequence disclosed herein for yk39_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts two potential transmembrane domains within the yk39_(—)1 protein sequence, one centered around amino acid 18 and another around amino acid 44 of SEQ ID NO:144. The nucleotide sequence of yk39_(—)1 indicates that it may contain a MIR repeat region.

Clone “yk91_(—)1”

A polynucleotide of the present invention has been identified as clone “yk91_(—)1”. yk91_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk91_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk91_(—)1 protein”).

The nucleotide sequence of yk91_(—)1 as presently determined is reported in SEQ ID NO:145, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk91_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:146. Amino acids 49 to 61 of SEQ ID NO:146 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 62. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk91_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk91_(—)1 should be approximately 1150 bp.

The nucleotide sequence disclosed herein for yk91_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts an additional potential transmembrane domain within the yk91_(—)1 protein sequence centered around amino acid 80 of SEQ ID NO:146. The nucleotide sequence of yk91_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yk199_(—)1”

A polynucleotide of the present invention has been identified as clone “yk199_(—)1”. yk199_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk199_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk199_(—)1 protein”).

The nucleotide sequence of yk199_(—)1 as presently determined is reported in SEQ ID NO:147, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk199_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:148. Amino acids 10 to 22 of SEQ ID NO:148 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 23. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk199_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk199_(—)1 should be approximately 1700 bp.

The nucleotide sequence disclosed herein for yk199_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk199_(—)1 demonstrated at least some similarity with sequences identified as AI039293 (ox33e12.s1 Soares_total_fetus_Nb2HF8_(—)9w Homo sapiens cDNA clone IMAGE:1658158 3′, mRNA sequence). Based upon sequence similarity, yk199_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yk199_(—)1 protein sequence, around amino acid 132 of SEQ ID NO:148. The nucleotide sequence and the predicted amino acid sequence of yk199_(—)1 indicate that it may contain human TAR1 (telomere-associated repeat 1) sequence.

Clone “yl4_(—)1”

A polynucleotide of the present invention has been identified as clone “yl4_(—)1”. yl4_(—)1 was isolated from a human adult spleen cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yl4_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yl4_(—)1 protein”).

The nucleotide sequence of yl4_(—)1 as presently determined is reported in SEQ ID NO:149, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yl4_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:150. Amino acids 204 to 216 of SEQ ID NO:150 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 217. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yl4_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yl4_(—)1 should be approximately 1250 bp.

The nucleotide sequence disclosed herein for yl4_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yl4_(—)1 demonstrated at least some similarity with sequences identified as AA283813 (zt19g10.s1 Soares ovary tumor NbHOT Homo sapiens cDNA clone 713634 3′, mRNA sequence). Based upon sequence similarity, yl4_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yl4_(—)1 protein sequence centered around amino acid 108 of SEQ ID NO:150.

Clone “yl14_(—)1”

A polynucleotide of the present invention has been identified as clone “yl14_(—)1”. yl14_(—)1 was isolated from a human adult spleen cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yl14_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yl14_(—)1 protein”).

The nucleotide sequence of yl14_(—)1 as presently determined is reported in SEQ ID NO:151, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yl14_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:152.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yl14_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yl14_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yl14_(—)1 demonstrated at least some similarity with sequences identified as AF034174 (Homo sapiens ntcon3 contig mRNA, partial sequence, mRNA sequence) and T03943 (human thrombopoietin genomic coding sequence). Based upon sequence similarity, yl14_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yl14_(—)1 protein sequence, one centered around amino acid 18 and another around amino acid 69 of SEQ ID NO:152; amino acids 61 to 73 are also a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 74 of SEQ ID NO:152. The nucleotide sequence of yl14_(—)1 indicates that it may contain an Alu repetitive element.

Clone “ya80_(—)1”

A polynucleotide of the present invention has been identified as clone “ya80_(—)1”. ya80_(—)1 was isolated from a human adult testes cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ya80_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ya80_(—)1 protein”).

The nucleotide sequence of ya80_(—)1 as presently determined is reported in SEQ ID NO:153, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ya80_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:154. Amino acids 31 to 43 of SEQ ID NO:154 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 44. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ya80_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ya80_(—)1 should be approximately 600 bp.

The nucleotide sequence disclosed herein for ya80_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts a potential transmembrane domain within the ya80_(—)1 protein sequence centered around amino acid 30 of SEQ ID NO:154.

Clone “yd61_(—)1”

A polynucleotide of the present invention has been identified as clone “yd61_(—)1”. yd61_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd61_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd61_(—)1 protein”).

The nucleotide sequence of yd61_(—)1 as presently determined is reported in SEQ ID NO:155, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd61_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:156. Amino acids 156 to 168 of SEQ ID NO:156 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 169. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd61_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd61_(—)1 should be approximately 950 bp.

The nucleotide sequence disclosed herein for yd61_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd61_(—)1 demonstrated at least some similarity with sequences identified as AI017161 (ou28a07.x1 Soares_NFL_T_GBC_S1 Homo sapiens cDNA clone IMAGE:1627572 3′ similar to TR:Q15040 Q15040 mRNA ;contains TAR1.t1 MSR1 repetitive element; mRNA sequence) and D31884 (Human mRNA for KIAA0063 gene, complete cds). The predicted amino acid sequence disclosed herein for yd61_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd61_(—)1 protein demonstrated at least some similarity to the sequence identified as D31884 (KIAA0063 [Homo sapiens]). Based upon sequence similarity, yd61_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yd61_(—)1 protein sequence, one centered around amino acid 78 and another around amino acid 11 of SEQ ID NO:156.

Clone “yd88_(—)1”

A polynucleotide of the present invention has been identified as clone “yd88_(—)1”. yd88_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd88_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd88_(—)1 protein”).

The nucleotide sequence of yd88_(—)1 as presently determined is reported in SEQ ID NO:157, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd88_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:158.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd88_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for yd88_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd88_(—)1 demonstrated at least some similarity with sequences identified as W22362 (66B4 Human retina cDNA Tsp509I-cleaved sublibrary Homo sapiens cDNA not directional, mRNA sequence). Based upon sequence similarity, yd88_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domains within the yd88_(—)1 protein sequence, around amino acid 60 of SEQ ID NO:158.

Clone “yd109_(—)1”

A polynucleotide of the present invention has been identified as clone “yd109_(—)1”. yd109_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd109_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd109_(—)1 protein”).

The nucleotide sequence of yd109_(—)1 as presently determined is reported in SEQ ID NO:159, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd109_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:160.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd109_(—)1 should be approximately 550 bp.

The nucleotide sequence disclosed herein for yd109_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd109_(—)1 demonstrated at least some similarity with sequences identified as AA809139 (nw17h06.s1 NCI_CGAP_GCBO Homo sapiens cDNA clone IMAGE:1240763, mRNA sequence) and T21990 (Human gene signature HUMGS03533; standard; cDNA to mRNA). The predicted amino acid sequence disclosed herein for yd109_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd109_(—)1 protein demonstrated at least some similarity to the sequence identified as U80438 (coded for by C. elegans cDNA CEESD64F; similar to a short region of DNAJ proteins in part of the DNAJ-like domain [Caenorhabditis elegans]). Based upon sequence similarity, yd109_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yd109_(—)1 protein sequence, centered around a position between amino acid 50 and amino acid 54 of SEQ ID NO:160.

Clone “yd141_(—)1”

A polynucleotide of the present invention has been identified as clone “yd141_(—)1”. yd141_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd141_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd141_(—)1 protein”).

The nucleotide sequence of yd141_(—)1 as presently determined is reported in SEQ ID NO:161, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd141_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:162.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd141_(—)1 should be approximately 650 bp.

The nucleotide sequence disclosed herein for yd141_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd141_(—)1 demonstrated at least some similarity with sequences identified as AA974564 (op28f05.s1 Soares_NFL_T_GBC_S1 Homo sapiens cDNA clone IMAGE 1578177 3′, mRNA sequence) and AC004789 (Homo sapiens chromosome 16, cosmid clone RT140 (LANL), complete sequence). Based upon sequence similarity, yd141_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts six potential transmembrane domains within the yd141_(—)1 protein sequence, one centered around amino acid 46 and others around amino acids 10, 35, 70, 93 and 100 of SEQ ID NO:162, respectively.

yd141_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 13 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yd153_(—)1”

A polynucleotide of the present invention has been identified as clone “yd153_(—)1”. yd153_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd153_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd153_(—)1 protein”).

The nucleotide sequence of yd153_(—)1 as presently determined is reported in SEQ ID NO:163, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd153_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:164. Amino acids 18 to 30 of SEQ ID NO:164 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 31. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd153_(—)1 protein.

Another potential yd153_(—)1 reading frame and predicted amino acid sequence is encoded by basepairs 68 to 244 of SEQ ID NO:163 and is reported in SEQ ID NO:268.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd153_(—)1 should be approximately 650 bp.

The nucleotide sequence disclosed herein for yd153_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd153_(—)1 demonstrated at least some similarity with sequences identified as AA309873 (EST180736 Jurkat T-cells V Homo sapiens cDNA 5′ end, mRNA sequence) and T26022 (Human gene signature HUMGS08258; standard; cDNA to mRNA). Based upon sequence similarity, yd153_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yd165_(—)1”

A polynucleotide of the present invention has been identified as clone “yd165_(—)1”. yd165_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd165_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd165_(—)1 protein”).

The nucleotide sequence of yd165_(—)1 as presently determined is reported in SEQ ID NO:165, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd165_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:166.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd165_(—)1 should be approximately 650 bp.

The nucleotide sequence disclosed herein for yd165_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd165_(—)1 demonstrated at least some similarity with sequences identified as AA873304 (oh75h10.s1 NCI_CGAP_Kid5 Homo sapiens cDNA clone IMAGE 1472899 3′ similar to SW INI7_HUMAN P40305 INTERFERON-ALPHA INDUCED 11.5 KD PROTEIN; mRNA sequence), V24016 (Human interferon-inducible protein, HIFI, coding sequence; standard; cDNA), and X67325 (H.sapiens p27 mRNA). The predicted amino acid sequence disclosed herein for yd165_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd165_(—)1 protein demonstrated at least some similarity to sequences identified as U22970 (interferon-inducible peptide precursor [Homo sapiens]), W54040 (Human interferon-inducible protein, HIFI), and X67325 (p27 gene product [Homo sapiens]). Based upon sequence similarity, yd165_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts three potential transmembrane domains within the yd165_(—)1 protein sequence, centered around amino acids 43, 77, and 107 of SEQ ID NO:166, respectively.

Clone “yd178_(—)1”

A polynucleotide of the present invention has been identified as clone “yd178_(—)1”. yd178_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd178_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd178_(—)1 protein”).

The nucleotide sequence of yd178_(—)1 as presently determined is reported in SEQ ID NO:167, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd178_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:168. Amino acids 7 to 19 of SEQ ID NO:168 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 20. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd178_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd178_(—)1 should be approximately 900 bp.

The nucleotide sequence disclosed herein for yd178_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd178_(—)1 demonstrated at least some similarity with sequences identified as AI141062 (oz43g12.x1 Soares_NhHMPu_S1 Homo sapiens cDNA clone IMAGE:1678150 3′ similar to SW:LYG_ANSAN P00718 LYSOZYME G; mRNA sequence) and X61002 (G.gallus mRNA for goose-type lysozyme). The predicted amino acid sequence disclosed herein for yd178_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yd178_(—)1 protein demonstrated at least some similarity to the sequence identified as X61002 (lysozyme [Gallus gallus]), and chicken “goose-type” lysozymes. Based upon sequence similarity, yd178_(—)1 proteins and each similar protein or peptide may share at least some activity.

yd178_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 23 kDa was detected in conditioned medium and membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yd191_(—)1”

A polynucleotide of the present invention has been identified as clone “yd191_(—)1”. yd191_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd191_(—)1 is a full-length done, including the entire coding sequence of a secreted protein (also referred to herein as “yd191_(—)1 protein”).

The nucleotide sequence of yd191_(—)1 as presently determined is reported in SEQ ID NO:169, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd191_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:170.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd191_(—)1 should be approximately 550 bp.

The nucleotide sequence disclosed herein for yd191_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd191_(—)1 demonstrated at least some similarity with sequences identified as H98768 (yx13d09.s1 Homo sapiens cDNA clone 261617 3′). Based upon sequence similarity, yd191_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the yd191_(—)1 protein sequence, one centered around amino acid 55 and another around amino acid 68 of SEQ ID NO:170.

Clone “ye7_(—)1”

A polynucleotide of the present invention has been identified as clone “ye7_(—)1”. ye7_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ye7_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ye7_(—)1 protein”).

The nucleotide sequence of ye7_(—)1 as presently determined is reported in SEQ ID NO:171, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ye7_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:172.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ye7_(—)1 should be approximately 2400 bp.

The nucleotide sequence disclosed herein for ye7_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ye7_(—)1 demonstrated at least some similarity with sequences identified as AI017060 (ov01d06.x1 NCI_CGAP_Kid3 Homo sapiens cDNA clone IMAGE:1636043 3′, mRNA sequence). Based upon sequence similarity, ye7_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two potential transmembrane domains within the ye7_(—)1 protein sequence, one centered around amino acid 65 and another around amino acid 105 of SEQ ID NO:172.

Clone “yf33_(—)1”

A polynucleotide of the present invention has been identified as clone “yf33_(—)1”. yf33_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yf33_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yf33_(—)1 protein”).

The nucleotide sequence of yf33_(—)1 as presently determined is reported in SEQ ID NO:173, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yf33_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:174. Amino acids 36 to 48 of SEQ ID NO:174 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 49. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yf33_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing done yf33_(—)1 should be approximately 2500 bp.

The nucleotide sequence disclosed herein for yf33_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts a potential transmembrane domain within the yf33_(—)1 protein sequence centered around amino acids 93 of SEQ ID NO:174. The nucleotide sequence of yf33_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yi15_(—)1”

A polynucleotide of the present invention has been identified as clone “yi15_(—)1”. yi15_(—)1 was isolated from a human brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi15_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi15_(—)1 protein”).

The nucleotide sequence of yi15_(—)1 as presently determined is reported in SEQ ID NO:175, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yi15_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:176. Amino acids 52 to 64 of SEQ ID NO:176 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 65. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi15_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi15_(—)1 should be approximately 2500 bp.

The nucleotide sequence disclosed herein for yi15_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi15_(—)1 demonstrated at least some similarity with sequences identified as AA290994 (zs45d07.r1 NCI_CGAP_GCB1 Homo sapiens cDNA clone IMAGE 700429 5′, mRNA sequence) and AF010235 (Homo sapiens mRNA from chromosome 5q31-33 region). Based upon sequence similarity, yi15_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts four potential transmembrane domains within the yi15_(—)1 protein sequence, centered around amino adds 30,60,70, and 100 of SEQ ID NO:176, respectively.

Clone “yi17_(—)1”

A polynucleotide of the present invention has been identified as clone “yi17_(—)1”. yi17_(—)1 was isolated from a human brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi17_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi17_(—)1 protein”).

The nucleotide sequence of yi17_(—)1 as presently determined is reported in SEQ ID NO:177, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yi17_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:178. Amino acids 6 to 18 of SEQ ID NO:178 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 19. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi17_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi17_(—)1 should be approximately 1700 bp.

The nucleotide sequence disclosed herein for yi17_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi17_(—)1 demonstrated at least some similarity with sequences identified as AA418852 (zw01f10.s1 Soares NhHMPu S1 Homo sapiens cDNA clone 768043 3′, mRNA sequence). Based upon sequence similarity, yi17_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yk38_(—)1”

A polynucleotide of the present invention has been identified as clone “yk38_(—)1”. yk38_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk38_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk38_(—)1 protein”).

The nucleotide sequence of yk38_(—)1 as presently determined is reported in SEQ ID NO:179, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk38_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:180. Amino acids 43 to 55 of SEQ ID NO:180 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 56. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk38_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk38_(—)1 should be approximately 2050 bp.

The nucleotide sequence disclosed herein for yk38_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk38_(—)1 demonstrated at least some similarity with sequences identified as AA477698 (zu44c09.r1 Soares ovary tumor NbHOT Homo sapiens cDNA clone 740848 5′, mRNA sequence), AF052183 (Homo sapiens clone 24804 mRNA sequence), and T26733 (Human gene signature HUMGS08983; standard; cDNA to mRNA). Based upon sequence similarity, yk38_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts four potential transmembrane domains within the yk38_(—)1 protein sequence, centered around amino acids 50, 135, 210 and 260 of SEQ ID NO:180, respectively. Hidden markov model and motifs analysis have revealed the presence of two WD-40 (beta transducin/G-beta) repeats at amino acids 118-153 and 157-196 of SEQ ID NO:180. The WD40 domain is thought to mediate protein-protein interactions.

Clone “yk51_(—)1”

A polynucleotide of the present invention has been identified as clone “yk51_(—)1”. yk51_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk51_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk51_(—)1 protein”).

The nucleotide sequence of yk51_(—)1 as presently determined is reported in SEQ ID NO:181, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk51_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:182. Amino acids 9 to 21 of SEQ ID NO:182 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 22. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk51_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk51_(—)1 should be approximately 1350 bp.

The nucleotide sequence disclosed herein for yk51_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk51_(—)1 demonstrated at least some similarity with sequences identified as Z93014 (Human DNA sequence *** SEQUENCING IN PROGRESS *** from clone 167P19; HTGS phase 1). Based upon sequence similarity, yk51_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yk51_(—)1 protein sequence, one centered around amino acid 65 and another around amino acid 81 of SEQ ID NO:182.

Clone “yk74_(—)1”

A polynucleotide of the present invention has been identified as clone “yk74_(—)1”. yk74_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk74_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk74_(—)1 protein”).

The nucleotide sequence of yk74_(—)1 as presently determined is reported in SEQ ID NO:183, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk74_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:184.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk74_(—)1 should be approximately 1500 bp.

The nucleotide sequence disclosed herein for yk74_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk74_(—)1 demonstrated at least some similarity with sequences identified as AA910887:(ok87e02.s1 NCI_CGAP_Lu5 Homo sapiens cDNA clone IMAGE:1520954 3′, mRNA sequence). Based upon sequence similarity, yk74_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts three potential transmembrane domains within the yk74_(—)1 protein sequence, centered around amino acids 15, 75, and 105 of SEQ ID NO:184, respectively. The nucleotide sequence of yk74_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yk89_(—)1”

A polynucleotide of the present invention has been identified as clone “yk89_(—)1”. yk89_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk89_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk89_(—)1 protein”).

The nucleotide sequence of yk89_(—)1 as presently determined is reported in SEQ ID NO:185, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk89_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:186.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk89_(—)1 should be approximately 2800 bp.

The nucleotide sequence disclosed herein for yk89_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk89_(—)1 demonstrated at least some similarity with sequences identified as AA524431 (ng44e05.s1 NCI_CGAP_Co3 Homo sapiens cDNA clone IMAGE 937664, mRNA sequence), AF045607 (Xenopus laevis origin recognition complex associated protein p81 mRNA, complete cds), U50950 (Human infant brain unknown product mRNA, complete cds), and V23269 (Human latheo protein encoding est cDNA; standard; cDNA). The predicted amino acid sequence disclosed herein for yk89_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yk89_(—)1 protein demonstrated at least some similarity to sequences identified as U50950 (unknown [Homo sapiens]), W53458 and W53460 (latheo protein [Drosophila]), W53459 (Human latheo protein sequence), and W53461 (Human latheo protein internal reading protein sequence). The latheo gene encodes a protein of ˜70 kD which lacks sequence or domain homology to known proteins. In situ staining with a polyclonal antibody raised against the Latheo protein reveals protein expression in the larval central nervous system (CNS), and specific localization in presynaptic boutons at roughly half the neuromuscular junctions in 3rd-instar larvae, consistent with a role for Latheo protein in synaptic function. (Rohrbough, Pinto, and Tully, Center for Learning and Memory, Cold Spring Harbor Laboratory; and K. S. Broadie, Dept. of Biology, University of Utah, Salt Lake City Utah 84112.) Based upon sequence similarity, yk89_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yk89_(—)1 protein sequence centered around amino acid 250 of SEQ ID NO:186.

Clone “yl18_(—)1”

A polynucleotide of the present invention has been identified as clone “yl18_(—)1”. yl18_(—)1 was isolated from a human adult spleen cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yl18_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yl18_(—)1 protein”).

The nucleotide sequence of yl18_(—)1 as presently determined is reported in SEQ ID NO:187, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yl18_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:188. Amino acids 13 to of SEQ ID NO:188 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 26. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yl18_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yl18_(—)1 should be approximately 3116 bp.

The nucleotide sequence disclosed herein for yl18_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yl18_(—)1 demonstrated at least some similarity with sequences identified as AA156907 (zl20b04.r1 Soares pregnant uterus NbHPU Homo sapiens cDNA clone 502447 5′, mRNA sequence). Based upon sequence similarity, yl18_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts three additional potential transmembrane domains within the yl18_(—)1 protein sequence, centered around amino acids 50, 105, and 115 of SEQ ID NO:188.

yl18_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 27 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “yb325_(—)1”

A polynucleotide of the present invention has been identified as clone “yb325_(—)1”. yb325_(—)1 was isolated from a human fetal brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yb325_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yb325_(—)1 protein”).

The nucleotide sequence of yb325_(—)1 as presently determined is reported in SEQ ID NO:189. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yb325_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:190. Amino acids 3 to 15 of SEQ ID NO:190 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 16. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yb325_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yb325_(—)1 should be approximately 839 bp.

The nucleotide sequence disclosed herein for yb325_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yb325_(—)1 demonstrated at least some similarity with sequences identified as AA523268 (ni39g02.s1 NCI_CGAP_Lu1 Homo sapiens cDNA clone IMAGE: 979250, mRNA sequence). Based upon sequence similarity, yb235_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts an additional potential transmembrane domain within the yb235_(—)1 protein sequence, centered around amino acid 90 of SEQ ID NO:188.

Clone “yd261_(—)1”

A polynucleotide of the present invention has been identified as clone “yd261_(—)1”. yd261_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yd261_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yd261_(—)1 protein”).

The nucleotide sequence of yd261_(—)1 as presently determined is reported in SEQ ID NO:191, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yd261_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:192. Amino acids 25 to 37 of SEQ ID NO:192 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 38. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yd261_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yd261_(—)1 should be approximately 491 bp.

The nucleotide sequence disclosed herein for yd261_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yd261_(—)1 demonstrated at least some similarity with sequences identified as Q61280 (Human brain Expressed Sequence Tag EST01297; standard; DNA) and T15557 (IB1543 Infant brain, Bento Soares Homo sapiens cDNA 3′ end similar to EST01297 H. sapiens cDNA clone HHCPN24, mRNA sequence). Based upon sequence similarity, yd261_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yh33_(—)1”

A polynucleotide of the present invention has been identified as clone “yh33_(—)1”. yh33_(—)1 was isolated from a human brain (fetal and adult) cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yh33_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yh33_(—)1 protein”).

The nucleotide sequence of yh33_(—)1 as presently determined is reported in SEQ ID NO:193, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yh33_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:194. Amino acids 80 to 92 of SEQ ID NO:194 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 93. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yh33_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yh33_(—)1 should be approximately 2750 bp.

The nucleotide sequence disclosed herein for yh33_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts three additional potential transmembrane domains within the yh33_(—)1 protein sequence, centered around amino acids 124, 160, and 190 of SEQ ID NO:194, respectively. The nucleotide sequence of yh33_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yi16_(—)1”

A polynucleotide of the present invention has been identified as clone “yi16_(—)1”. yi16_(—)1 was isolated from a human adult brain cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yi16_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yi16_(—)1 protein”).

The nucleotide sequence of yi16_(—)1 as presently determined is reported in SEQ ID NO:195, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yi16_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:196. Amino acids 63 to 75 of SEQ ID NO:196 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 76. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yi16_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yi16_(—)1 should be approximately 3000 bp.

The nucleotide sequence disclosed herein for yi16_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yi16_(—)1 demonstrated at least some similarity with sequences identified as AI076775 (oz31f03.x1 Soares_total_fetus_Nb2HF8_(—)9w Homo sapiens cDNA clone IMAGE 1676957 3′, mRNA sequence), T19914 (Human gene signature HUMGS01041; standard; cDNA to mRNA), and U79267 (Human clone 23840 mRNA, partial cds). The predicted amino acid sequence disclosed herein for yi16_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yi16_(—)1 protein demonstrated at least some similarity to the sequence identified as U79267 (unknown [Homo sapiens]). Based upon sequence similarity, yi16_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yk46_(—)1”

A polynucleotide of the present invention has been identified as clone “yk46_(—)1”. yk46_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk46_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk46_(—)1 protein”).

The nucleotide sequence of yk46_(—)1 as presently determined is reported in SEQ ID NO:197, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk46_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:198. Amino acids 28 to 40 of SEQ ID NO:198 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 41. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk46_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk46_(—)1 should be approximately 1900 bp.

The nucleotide sequence disclosed herein for yk46_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk46_(—)1 demonstrated at least some similarity with sequences identified as AA203346 (zx56h01.r1 Soares fetal liver spleen 1NFLS S1 Homo sapiens cDNA clone 446545 5′, mRNA sequence). Based upon sequence similarity, yk46_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yk46_(—)1 protein sequence, one centered around amino acid 20 and another around amino acid 57 of SEQ ID NO:198.

Clone “yk84_(—)1”

A polynucleotide of the present invention has been identified as clone “yk84_(—)1”. yk84_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk84_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk84_(—)1 protein”).

The nucleotide sequence of yk84_(—)1 as presently determined is reported in SEQ ID NO:199, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk84_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:200. Amino acids 36 to 48 of SEQ ID NO:200 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 49. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk84_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk84_(—)1 should be approximately 2400 bp.

The nucleotide sequence disclosed herein for yk84_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk84_(—)1 demonstrated at least some similarity with sequences identified as AC004052 (Homo sapiens chromosome 4 clone B209B10 map 4q25, complete sequence) and AQ0059417 (CIT-HSP-2348J2.TF CIT-HSP Homo sapiens genomic clone 2348J2, genomic survey sequence). Based upon sequence similarity, yk84_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts a potential transmembrane domain within the yk84_(—)1 protein sequence, centered around amino acid 49 of SEQ ID NO:200.

Clone “yk143_(—)1”

A polynucleotide of the present invention has been identified as clone “yk143_(—)1”. yk143_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk143_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk143_(—)1 protein”).

The nucleotide sequence of yk143_(—)1 as presently determined is reported in SEQ ID NO:201, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk143_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:202. Amino acids 31 to 43 of SEQ ID NO:202 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 44. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk143_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk143_(—)1 should be approximately 1458 bp.

The nucleotide sequence disclosed herein for yk143_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk143_(—)1 demonstrated at least some similarity with sequences identified as AA526186 (ni94h03.s1 NCI_CGAP_Pr21 Homo sapiens cDNA clone IMAGE:984533, mRNA sequence), AB006085 (Danio rerio mRNA for MINDIN2, complete cds), and T78360 (Human neuronal attachment factor-1 DNA; standard; DNA). The predicted amino acid sequence disclosed herein for yk143_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yk143_(—)1 protein demonstrated at least some similarity to sequences identified as AB006085 (MINDIN2 [Danio rerio]) and W23663 (Human neuronal attachment factor-1). Human neuronal attachment factor-1 is thought to promote cell-cell interaction and cell adhesion. The predicted yk143_(—)1 protein also demonstrated at least some similarity to the extracellular matrix proteins called F- and M-spodins. Based upon sequence similarity, yk143_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yk143_(—)1 protein sequence, one centered around amino acid 204 and another around amino acid 280 of SEQ ID NO:202.

Clone “yk156_(—)1”

A polynucleotide of the present invention has been identified as clone “yk156_(—)1”. yk156_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk156_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk156_(—)1 protein”).

The nucleotide sequence of yk156_(—)1 as presently determined is reported in SEQ ID NO:203, and indudes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk156_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:204. Amino acids 25 to 37 of SEQ ID NO:204 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 38. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk156_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing done yk156_(—)1 should be approximately 1100 bp.

The nucleotide sequence disclosed herein for yk156_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk156_(—)1 demonstrated at least some similarity with sequences identified as AC002550 (Human Chromosome 16 BAC clone CIT987SK-A-101F10, complete sequence) and N67878 (yz52b04.s1 Homo sapiens cDNA clone 286639 3′ similar to gb M29610 GLYCOPHORIN E PRECURSOR (HUMAN)). Based upon sequence similarity, yk156_(—)1 proteins and each similar protein or peptide may share at least some activity.

Clone “yk204_(—)1”

A polynucleotide of the present invention has been identified as clone “yk204_(—)1”. yk204_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk204_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk204_(—)1 protein”).

The nucleotide sequence of yk204_(—)1 as presently determined is reported in SEQ ID NO:205, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk204_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:206. Amino acids 46 to 58 of SEQ ID NO:206 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 59. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk204_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk204_(—)1 should be approximately 1395 bp.

The nucleotide sequence disclosed herein for yk204_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. No significant hits were found in the database. The TopPredII computer program predicts two potential transmembrane domains within the yk204_(—)1 protein sequence, one centered around amino acid 59 and another around amino acid 82 of SEQ ID NO:206. The nucleotide sequence of yk204_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yk224_(—)1”

A polynucleotide of the present invention has been identified as clone “yk224_(—)1”. yk224_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk224_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk224_(—)1 protein”).

The nucleotide sequence of yk224_(—)1 as presently determined is reported in SEQ ID NO:207, and indudes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk224_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:208. Amino acids 13 to 25 of SEQ ID NO:208 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 26. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk224_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk224_(—)1 should be approximately 1600 bp.

The nucleotide sequence disclosed herein for yk224_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk224_(—)1 demonstrated at least some similarity with sequences identified as AA789332 (aj28h05.s1 Soares testis NHT Homo sapiens cDNA clone 1391673 3′ similar to WP:B0410.2 CE06708; mRNA sequence) and AF044208 (Drosophila melanogaster Strabismus (stbm) mRNA, complete cds). The predicted amino acid sequence disclosed herein for yk224_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yk224_(—)1 protein demonstrated at least some similarity to the sequence identified as AF044208 (Strabismus [Drosophila melanogaster]). Strabismus is described as a protein “that regulates tissue polarity and cell fate decisions in Drosophila” (Wolff, T. and Rubin, G. M., 1998, Development 125(6): 1149-1159, which is incorporated by reference herein). Based upon sequence similarity, yk224_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts four potential transmembrane domains within the yk224_(—)1 protein sequence, centered around amino acids 26, 64, 98, and 134 of SEQ ID NO:208, respectively. The nucleotide sequence of yk224_(—)1 indicates that it may contain an Alu repetitive element.

Clone “yk261_(—)1”

A polynucleotide of the present invention has been identified as clone “yk261_(—)1”. yk261_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. yk261_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “yk261_(—)1 protein”).

The nucleotide sequence of yk261_(—)1 as presently determined is reported in SEQ ID NO:209, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the yk261_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:210. Amino acids 13 to 25 of SEQ ID NO:210 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 26. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the yk261_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone yk261_(—)1 should be approximately 2259 bp.

The nucleotide sequence disclosed herein for yk261_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. yk261_(—)1 demonstrated at least some similarity with sequences identified as AI024733 (ov76e12.x1 Soares_testis_NHT Homo sapiens cDNA clone IMAGE:1643278 3′, mRNA sequence). The predicted amino acid sequence disclosed herein for yk261_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted yk261_(—)1 protein demonstrated at least some similarity to sequences identified as AF040650 (contains similarity to sodium-potassium-chloride cotransport proteins [Caenorhabditis elegans]), AF051561 (similarity to sodium-potassium chloride cotransport proteins [rat]), U13174 (putative basolateral Na-K-2Cl cotransporter [Mus musculus]), U55054 (K-Cl cotransporter [Homo sapiens]), and Z36104 (similarity to sodium-potassium-chloride cotransport proteins [yeast]). Based upon sequence similarity, yk261_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts two additional potential transmembrane domains within the yk261_(—)1 protein sequence, one centered around amino acid 270 and another around amino acid 295 of SEQ ID NO:210.

Clone “ys3_(—)1”

A polynucleotide of the present invention has been identified as clone “ys3_(—)1”. ys3_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ys3_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ys3_(—)1 protein”).

The nucleotide sequence of ys3_(—)1 as presently determined is reported in SEQ ID NO:211, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ys3_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:212. Amino acids 112 to 124 of SEQ ID NO:212 are a possible leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 125. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ys3_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ys3_(—)1 should be approximately 1000 bp.

The nucleotide sequence disclosed herein for ys3_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ys3_(—)1 demonstrated at least some similarity with sequences identified as H93009 (yv07g03.s1 Homo sapiens cDNA clone 242068 3′). The predicted amino acid sequence disclosed herein for ys3_(—)1 was searched against the GenPept and GeneSeq amino acid sequence databases using the BLASTX search protocol. The predicted ys3_(—)1 protein demonstrated at least some similarity to sequences identified as L35848 (IgE receptor beta subunit [Homo sapiens]) and R42337 (Human FceRI beta). Based upon sequence similarity, ys3_(—)1 proteins and each similar protein or peptide may share at least some activity. The TopPredII computer program predicts five potential transmembrane domains within the ys3_(—)1 protein sequence, centered around amino acids 60, 90, 125, 190, and 225 of SEQ ID NO:212, respectively.

ys3_(—)1 protein was expressed in a COS cell expression system, and an expressed protein band of approximately 26 kDa was detected in membrane fractions using SDS polyacrylamide gel electrophoresis.

Clone “ys10_(—)1”

A polynucleotide of the present invention has been identified as clone “ys10_(—)1”. ys10_(—)1 was isolated from a human adult thymus cDNA library and was identified as encoding a secreted or transmembrane protein on the basis of computer analysis of the amino acid sequence of the encoded protein. ys10_(—)1 is a full-length clone, including the entire coding sequence of a secreted protein (also referred to herein as “ys10_(—)1 protein”).

The nucleotide sequence of ys10_(—)1 as presently determined is reported in SEQ ID NO:213, and includes a poly(A) tail. What applicants presently believe to be the proper reading frame and the predicted amino acid sequence of the ys10_(—)1 protein corresponding to the foregoing nucleotide sequence is reported in SEQ ID NO:214. Amino acids 30 to 42 of SEQ ID NO:214 are a predicted leader/signal sequence, with the predicted mature amino acid sequence beginning at amino acid 43. Due to the hydrophobic nature of the predicted leader/signal sequence, it is likely to act as a transmembrane domain should the predicted leader/signal sequence not be separated from the remainder of the ys10_(—)1 protein.

The EcoRI/NotI restriction fragment obtainable from the deposit containing clone ys10_(—)1 should be approximately 1079 bp.

The nucleotide sequence disclosed herein for ys10_(—)1 was searched against the GenBank and GeneSeq nucleotide sequence databases using BLASTN/BLASTX and FASTA search protocols. ys10_(—)1 demonstrated at least some similarity with sequences identified as AA436002 (zu03b10.s1 Soares testis NHT Homo sapiens cDNA clone 730747 3′, mRNA sequence) and T26591 (Human gene signature HUMGS08837; standard; cDNA to mRNA). Based upon sequence similarity, ys10_(—)1 proteins and each similar protein or peptide may share at least some activity.

Deposit of Clones

Clones ya15_(—)1, ya24_(—)1, yb42_(—)1, yc9_(—)1, yc19_(—)1, and yc20_(—)1 were deposited on Feb. 11, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98650, from which each clone comprising a particular polynucleotide is obtainable.

Clones ya9_(—)1, ya11_(—)1, ya28_(—)1, yb81_(—)1, and yc14_(—)1 were deposited on Apr. 7, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98724, from which each clone comprising a particular polynucleotide is obtainable.

Clones yc24_(—)1, yc25_(—)1, and ye2_(—)1 were deposited on May 14, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98755, from which each clone comprising a particular polynucleotide is obtainable.

Clones ya65_(—)1, yb60_(—)1, yb139_(—)1, yc29_(—)1, yc40_(—)1, yd10_(—)1, and yf5_(—)1 were deposited on Aug. 11, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98834, from which each clone comprising a particular polynucleotide is obtainable.

Clones ya67_(—)1, ya70_(—)1, yb51_(—)1, yb101_(—)1, yb124_(—)1, yb125_(—)1, yb179_(—)1, yc48_(—)1, ye21_(—)1, and ye22_(—)1 were deposited on Sep. 3, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98864, from which each clone comprising a particular polynucleotide is obtainable.

Clones ye39_(—)1, yf9_(—)1, yh4_(—)1, yi4_(—)1, yj3_(—)1, yj7_(—)1, yj10_(—)1, yj28_(—)1, yj29_(—)1, and yj32_(—)1 were deposited on Sep. 2, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98861, from which each clone comprising a particular polynucleotide is obtainable.

Clones yb186_(—)1, yb226_(—)1, yd50_(—)1, yd51_(—)1, yd73_(—)1, ye43_(—)1, yh71_(—)1, yj100_(—)1, yi3_(—)1, yj23_(—)1, and yl9_(—)1 were deposited on Sep. 10, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98872, from which each clone comprising a particular polynucleotide is obtainable.

Clones ya66_(—)1, yb187_(—)1, yb219_(—)1, yb228_(—)1, yc27_(—)1, yc49_(—)1, yd40_(—)1, yd64_(—)1, ye47_(—)1, yh50_(—)1, yh53_(—)1, and yh98_(—)1 were deposited on Sep. 23, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number. ATCC 98887, from which each clone comprising a particular polynucleotide is obtainable.

Clones ya69_(—)1, yd107_(—)1, yd145_(—)1, yh24_(—)1, yi11_(—)1, yi18_(—)1, yk14_(—)1, yk39_(—)1, yk91_(—)1, yk199_(—)1, yl4_(—)1, and yl14_(—)1 were deposited on Oct. 6, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98915, from which each clone comprising a particular polynucleotide is obtainable.

Clones ya80_(—)1, yd61_(—)1, yd88_(—)1, yd109_(—)1, yd141_(—)1, yd153_(—)1, yd165_(—)1, yd178_(—)1, and yd191_(—)1 were deposited on Oct. 15, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98925, from which each clone comprising a particular polynucleotide is obtainable.

Clones ye7_(—)1, yf33_(—)1, yi15_(—)1, yi17_(—)1, yk38_(—)1, yk51_(—)1, yk74_(—)1, yk89_(—)1, yk18_(—)1 were deposited on Oct. 15, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98924, from which each clone comprising a particular polynucleotide is obtainable.

Clones yb235_(—)1, yd261_(—)1, yh33_(—)1, yi16_(—)1, yk46_(—)1, yk84_(—)1, yk143_(—)1, yk156_(—)1, yk204_(—)1, yk224_(—)1, yk261_(—)1, ys3_(—)1, and ys10_(—)1 were deposited on Oct. 27, 1998 with the American Type Culture Collection (10801 University Boulevard, Manassas, Va. 20110-2209 U.S.A.) as an original deposit under the Budapest Treaty and were given the accession number ATCC 98958, from which each clone comprising a particular polynucleotide is obtainable.

All restrictions on the availability to the public of the deposited material will be irrevocably removed upon the granting of the patent, except for the requirements specified in 37 C.F.R. § 1.808(b), and the term of the deposit will comply with 37 C.F.R. § 1.806.

Each clone has been transfected into separate bacterial cells (E. coli) in these composite deposits. Each clone can be removed from the vector in which it was deposited by performing an EcoRI/NotI digestion (5′ site, EcoRI; 3′ site, NotI) to produce the appropriate fragment for such clone. Each clone was deposited in either the pED6 or pNOTs vector depicted in FIGS. 1A and 1B, respectively. The pED6dpc2 vector (“pED6”) was derived from pED6dpc1 by insertion of a new polylinker to facilitate cDNA cloning (Kaufman et al., 1991, Nucleic Acids Res. 19: 4485-4490); the pNOTs vector was derived from pMT2 (Kaufman et al., 1989, Mol. Cell. Biol. 9: 946-958) by deletion of the DHFR sequences, insertion of a new polylinker, and insertion of the M13 origin of replication in the ClaI site. In some instances, the deposited clone can become “flipped” (i.e., in the reverse orientation) in the deposited isolate. In such instances, the cDNA insert can still be isolated by digestion with EcoRI and NotI. However, NotI will then produce the 5′ site and EcoRI will produce the 3′ site for placement of the cDNA in proper orientation for expression in a suitable vector. The cDNA may also be expressed from the vectors in which they were deposited.

Bacterial cells containing a particular clone can be obtained from the composite deposit as follows:

An oligonucleotide probe or probes should be designed to the sequence that is known for that particular clone. This sequence can be derived from the sequences provided herein, or from a combination of those sequences. The sequence of an oligonucleotide probe that was used to isolate or to sequence each full-length clone is identified below, and should be most reliable in isolating the clone of interest.

Clone Probe Sequence ya15_1 SEQ ID NO:215 ya24_1 SEQ ID NO:216 yb42_1 SEQ ID NO:217 yc9_1 SEQ ID NO:218 yc19_1 SEQ ID NO:219 yc20_1 SEQ ID NO:220 ya9_1 SEQ ID NO:221 ya28_1 SEQ ID NO:222 yc14_1 SEQ ID NO:223 yc24_1 SEQ ID NO:224 yc25_1 SEQ ID NO:225 ye2_1 SEQ ID NO:226 yb60_1 SEQ ID NO:227 yc29_1 SEQ ID NO:228 yf5_1 SEQ ID NO:229 ya70_1 SEQ ID NO:230 yb51_1 SEQ ID NO:231 yb101_1 SEQ ID NO:232 yb124_1 SEQ ID NO:233 yb125_1 SEQ ID NO:234 yb179_1 SEQ ID NO:235 ye21_1 SEQ ID NO:236 ye22_1 SEQ ID NO:237 yf9_1 SEQ ID NO:238 yh71_1 SEQ ID NO:239 yh100_1 SEQ ID NO:240 yj23_1 SEQ ID NO:241 yb187_1 SEQ ID NO:242 yb219_1 SEQ ID NO:243 yd40_1 SEQ ID NO:244 ye47_1 SEQ ID NO:245 yh50_1 SEQ ID NO:246 yh53_1 SEQ ID NO:247 ya69_1 SEQ ID NO:248 yi11_1 SEQ ID NO:249 yl4_1 SEQ ID NO:250 ye7_1 SEQ ID NO:251 yf33_1 SEQ ID NO:252 yi15_1 SEQ ID NO:253 yi17_1 SEQ ID NO:254 yk38_1 SEQ ID NO:255 yk89_1 SEQ ID NO:256 yl18_1 SEQ ID NO:257 yh33_1 SEQ ID NO:258 yi16_1 SEQ ID NO:259 yk46_1 SEQ ID NO:260 yk84_1 SEQ ID NO:261 yk204_1 SEQ ID NO:262 yk224_1 SEQ ID NO:263 yk261_1 SEQ ID NO:264

In the sequences listed above which include an N at position 2, that position is occupied in preferred probes/primers by a biotinylated phosphoaramidite residue rather than a nucleotide (such as, for example, that produced by use of biotin phosphoramidite (1-dimethoxytrityloxy-2-(N-biotinyl-4-aminobutyl)-propyl-3-O-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramadite) (Glen Research, cat; no. 10-1953)).

The design of the oligonucleotide probe should preferably follow these parameters:

(a) It should be designed to an area of the sequence which has the fewest ambiguous bases (“N's”), if any;

(b) It should be designed to have a T_(m) of approx. 80° C. (assuming 2° for each A or T and 4 degrees for each G or C).

The oligonucleotide should preferably be labeled with γ-³²P ATP (specific activity 6000 Ci/mmole) and T4 polynucleotide kinase using commonly employed techniques for labeling oligonucleotides. Other labeling techniques can also be used. Unincorporated label should preferably be removed by gel filtration chromatography or other established methods. The amount of radioactivity incorporated into the probe should be quantitated by measurement in a scintillation counter. Preferably, specific activity of the resulting probe should be approximately 4e+6 dpm/pmole.

The bacterial culture containing the pool of full-length clones should preferably be thawed and 100 μl of the stock used to inoculate a sterile culture flask containing 25 ml of sterile L-broth containing ampicillin at 100 μg/ml. The culture should preferably be grown to saturation at 37° C., and the saturated culture should preferably be diluted in fresh L-broth. Aliquots of these dilutions should preferably be plated to determine the dilution and volume which will yield approximately 5000 distinct and well-separated colonies on solid bacteriological media containing L-broth containing ampicillin at 100 μg/ml and agar at 1.5% in a 150 mm petri dish when grown overnight at 37° C. Other known methods of obtaining distinct, well-separated colonies can also be employed.

Standard colony hybridization procedures should then be used to transfer the colonies to nitrocellulose filters and lyse, denature and bake them.

The filter is then preferably incubated at 65° C. for 1 hour with gentle agitation in 6×SSC (20×stock is 175.3 g NaCl/liter, 88.2 g Na citrate/liter, adjusted to pH 7.0 with NaOH) containing 0.5% SDS, 100 μg/ml of yeast RNA, and 10 mM EDTA (approximately 10 mL per 150 mm filter). Preferably, the probe is then added to the hybridization mix at a concentration greater than or equal to 1e+6 dpm/mL. The filter is then preferably incubated at 65° C. with gentle agitation overnight. The filter is then preferably washed in 500 mL of 2×SSC/0.5% SDS at room temperature without agitation, preferably followed by 500 mL of 2×SSC/0.1% SDS at room temperature with gentle shaking for 15 minutes. A third wash with 0.1×SSC/0.5% SDS at 65° C. for 30 minutes to 1 hour is optional. The filter is then preferably dried and subjected to autoradiography for sufficient time to visualize the positives on the X-ray film. Other known hybridization methods can also be employed.

The positive colonies are picked, grown in culture, and plasmid DNA isolated using standard procedures. The clones can then be verified by restriction analysis, hybridization analysis, or DNA sequencing.

Fragments of the proteins of the present invention which are capable of exhibiting biological activity are also encompassed by the present invention. Fragments of the protein may be in linear form or they maybe cyclized using known methods, for example, as described in H. U. Saragovi, et al., Bio/Technology 10, 773-778 (1992) and in R. S. McDowell, et al., J. Amer. Chem. Soc. 114, 9245-9253 (1992), both of which are incorporated herein by reference. Such fragments may be fused to carrier molecules such as immunoglobulins for many purposes, including increasing the valency of protein binding sites. For example, fragments of the protein may be fused through “linker” sequences to the Fc portion of an immunoglobulin. For a bivalent form of the protein, such a fusion could be to the Fc portion of an IgG molecule. Other immunoglobulin isotypes may also be used to generate such fusions. For example, a protein—IgM fusion would generate a decavalent form of the protein of the invention.

The present invention also provides both full-length and mature forms of the disclosed proteins. The full-length form of the such proteins is identified in the sequence listing by translation of the nucleotide sequence of each disclosed clone. The mature form(s) of such protein may be obtained by expression of the disclosed full-length polynucleotide (preferably those deposited with ATCC) in a suitable mammalian cell or other host cell. The sequence(s) of the mature form(s) of the protein may also be determinable from the amino acid sequence of the full-length form.

The present invention also provides genes corresponding to the polynucleotide sequences disclosed herein. “Corresponding genes” are the regions of the genome that are transcribed to produce the mRNAs from which cDNA polynucleotide sequences are derived and may include contiguous regions of the genome necessary for the regulated expression of such genes. Corresponding genes may therefore include but are not limited to coding sequences, 5′ and 3′ untranslated regions, alternatively spliced exons, introns, promoters, enhancers, and silencer or suppressor elements. The corresponding genes can be isolated in accordance with known methods using the sequence information disclosed herein. Such methods include the preparation of probes or primers from the disclosed sequence information for identification and/or amplification of genes in appropriate genomic libraries or other sources of genomic materials. An “isolated gene” is a gene that has been separated from the adjacent coding sequences, if any, present in the genome of the organism from which the gene was isolated.

The chromosomal location corresponding to the polynucleotide sequences disclosed herein may also be determined, for example by hybridizing appropriately labeled polynucleotides of the present invention to chromosomes in situ. It may also be possible to determine the corresponding chromosomal location for a disclosed polynucleotide by identifying significantly similar nucleotide sequences in public databases, such as expressed sequence tags (ESTs), that have already been mapped to particular chromosomal locations. For at least some of the polynucleotide sequences disclosed herein, public database sequences having at least some similarity to the polynucleotide of the present invention have been listed by database accession number. Searches using the GenBank accession numbers of these public database sequences can then be performed at an Internet site provided by the National Center for Biotechnology Information having the address http://www.ncbi.nlm.nih.gov/UniGene/, in order to identify “UniGene clusters” of overlapping sequences. Many of the “UniGene clusters” so identified will already have been mapped to particular chromosomal sites.

Organisms that have enhanced, reduced, or modified expression of the gene(s) corresponding to the polynucleotide sequences disclosed herein are provided. The desired change in gene expression can be achieved through the use of antisense polynucleotides or ribozymes that bind and/or cleave the mRNA transcribed from the gene (Albert and Morris, 1994, Trends Pharmacol. Sci. 15(7): 250-254; Lavarosky et al., 1997, Biochem. Mol. Med. 62(1): 11-22; and Hampel, 1998, Prog. Nucleic Acid Res. Mol. Biol. 58: 1-39; all of which are incorporated by reference herein). Transgenic animals that have multiple copies of the gene(s) corresponding to the polynucleotide sequences disclosed herein, preferably produced by transformation of cells with genetic constructs that are stably maintained within the transformed cells and their progeny, are provided.

Transgenic animals that have modified genetic control regions that increase or reduce gene expression levels, or that change temporal or spatial patterns of gene expression, are also provided (see European Patent No. 0 649 464 B1, incorporated by reference herein).

In addition, organisms are provided in which the gene(s) corresponding to the polynucleotide sequences disclosed herein have been partially or completely inactivated, through insertion of extraneous sequences into the corresponding gene(s) or through deletion of all or part of the corresponding gene(s). Partial or complete gene inactivation can be accomplished through insertion, preferably followed by imprecise excision, of transposable elements (Plasterk, 1992, Bioessays 14(9): 629-633; Zwaal et al., 1993, Proc. Natl. Acad. Sci. USA 90(16): 7431-7435; Clark et al., 1994, Proc. Natl. Acad. Sci. USA 91(2): 719-722; all of which are incorporated by reference herein), or through homologous recombination, preferably detected by positive/negative genetic selection strategies (Mansour et al., 1988, Nature 336: 348-352; U.S. Pat. Nos. 5,464,764; 5,487,992; 5,627,059; 5,631,153; 5,614,396; 5,616,491; and 5,679,523; all of which are incorporated by reference herein). These organisms with altered gene expression are preferably eukaryotes and more preferably are mammals. Such organisms are useful for the development of non-human models for the study of disorders involving the corresponding gene(s), and for the development of assay systems for the identification of molecules that interact with the protein product(s) of the corresponding gene(s).

Where the protein of the present invention is membrane-bound (e.g., is a receptor), the present invention also provides for soluble forms of such protein. In such forms, part or all of the intracellular and transmembrane domains of the protein are deleted such that the protein is fully secreted from the cell in which it is expressed. The intracellular and transmembrane domains of proteins of the invention can be identified in accordance with known techniques for determination of such domains from sequence information. For example, the TopPredII computer program can be used to predict the location of transmembrane domains in an amino acid sequence, domains which are described by the location of the center of the transmsmbrane domain, with at least ten transmembrane amino acids on each side of the reported central residue(s).

Proteins and protein fragments of the present invention include proteins with amino acid sequence lengths that are at least 25%(more preferably at least 50%, and most preferably at least 75%) of the length of a disclosed protein and have at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% or 95% identity) with that disclosed protein, where sequence identity is determined by comparing the amino acid sequences of the proteins when aligned so as to maximize overlap and identity while minimizing sequence gaps. Also included in the present invention are proteins and protein fragments that contain a segment preferably comprising 8 or more (more preferably 20 or more, most preferably 30 or more) contiguous amino acids that shares at least 75% sequence identity (more preferably, at least 85% identity; most preferably at least 95% identity) with any such segment of any of the disclosed proteins.

In particular, sequence identity may be determined using WU-BLAST (Washington University BLAST) version 2.0 software, which builds upon WU-BLAST version 1.4, which in turn is based on the public domain NCBI-BLAST version 1.4 (Altschul and Gish, 1996, Local alignment statistics, Doolittle ed., Methods in Enzymology 266: 460-480; Altschul et al., 1990, Basic local alignment search tool, Journal of Molecular Biology 215: 403-410; Gish and States, 1993, Identification of protein coding regions by database similarity search, Nature Genetics 3: 266-272; Karlin and Altschul, 1993, Applications and statistics for multiple high-scoring segments in molecular sequences, Proc. Natl. Acad. Sci. USA 90: 5873-5877; all of which are incorporated by reference herein). WU-BLAST version 2.0 executable programs for several UNIX platforms can be downloaded from ftp://blast.wustl.edu/blast/executables. The complete suite of search programs (BLASTP, BLASTN, BLASTX, TBLASTN, and TBLASTX) is provided at that site, in addition to several support programs. WU-BLAST 2.0 is copyrighted and may not be sold or redistributed in any form or manner without the express written consent of the author; but the posted executables may otherwise be freely used for commercial, nonprofit, or academic purposes. In all search programs in the suite—BLASTP, BLASTN, BLASTX, TBLASTN and TBLASTX—the gapped alignment routines are integral to the database search itself, and thus yield much better sensitivity and selectivity while producing the more easily interpreted output. Gapping can optionally be turned off in all of these programs, if desired. The default penalty (Q) for a gap of length one is Q=9 for proteins and BLASTP, and Q=10 for BLASTN, but may be changed to any integer value including zero, one through eight, nine, ten, eleven, twelve through twenty, twenty-one through fifty, fifty-one through one hundred, etc. The default per-residue penalty for extending a gap (R) is R=2 for proteins and BLASTP, and R=10 for BLASTN, but may be changed to any integer value including zero, one, two, three, four, five, six, seven, eight, nine, ten, eleven, twelve through twenty, twenty-one through fifty, fifty-one through one hundred, etc. Any combination of values for Q and R can be used in order to align sequences so as to maximize overlap and identity while minimizing sequence gaps. The default amino acid comparison matrix is BLOSUM62, but other amino acid comparison matrices such as PAM can be utilized.

Species homologues of the disclosed polynucleotides and proteins are also provided by the present invention. As used herein, a “species homologue” is a protein or polynucleotide with a different species of origin from that of a given protein or polynucleotide, but with significant sequence similarity to the given protein or polynucleotide. Preferably, polynucleotide species homologues have at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% identity) with the given polynucleotide, and protein species homologues have at least 30% sequence identity (more preferably, at least 45% identity; most preferably at least 60% identity) with the given protein, where sequence identity is determined by comparing the nucleotide sequences of the polynucleotides or the amino acid sequences of the proteins when aligned so as to maximize overlap and identity while minimizing sequence gaps. Species homologues may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source from the desired species. Preferably, species homologues are those isolated from mammalian species. Most preferably, species homologues are those isolated from certain mammalian species such as, for example, Pan troglodytes, Gorilla gorilla, Pongo pygmaeus, Hylobates concolor, Macaca mulatta, Papio papio, Papio hamadryas, Cercopithecus aethiops, Cebus capucinus, Aotus trivirgatus, Sanguinus oedipus, Microcebus murinus, Mus musculus, Rattus norvegicus, Cricetulus griseus, Felis catus, Mustela vzison, Canis familiaris, Oryctolagus cuniculus, Bos taurus, Ovis aries, Sus scrofa, and Equus caballus, for which genetic maps have been created allowing the identification of syntenic relationships between the genomic organization of genes in one species and the genomic organization of the related genes in another species (O'Brien and Seuanez, 1988, Ann. Rev. Genet. 22: 323-351; O'Brien et al., 1993, Nature Genetics 3:103-112; Johansson et al., 1995, Genomics 25: 682-690; Lyons et al., 1997, Nature Genetics 15:47-56; O'Brien et al., 1997, Trends in Genetics 13(10): 393-399; Carver and Stubbs, 1997, Genome Research 7:1123-1137; all of which are incorporated by reference herein).

The invention also encompasses allelic variants of the disclosed polynucleotides or proteins; that is, naturally-occurring alternative forms of the isolated polynucleotides which also encode proteins which are identical or have significantly similar sequences to those encoded by the disclosed polynucleotides. Preferably, allelic variants have at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% identity) with the given polynucleotide, where sequence identity is determined by comparing the nucleotide sequences of the polynucleotides when aligned so as to maximize overlap and identity while minimizing sequence gaps. Allelic variants may be isolated and identified by making suitable probes or primers from the sequences provided herein and screening a suitable nucleic acid source from individuals of the appropriate species.

The invention also includes polynucleotides with sequences complementary to those of the polynucleotides disclosed herein.

The present invention also includes polynucleotides that hybridize under reduced stringency conditions, more preferably stringent conditions, and most preferably highly stringent conditions, to polynucleotides described herein. Examples of stringency conditions are shown in the table below: highly stringent conditions are those that are at least as stringent as, for example, conditions A-F; stringent conditions are at least as stringent as, for example, conditions G-L; and reduced stringency conditions are at least as stringent as, for example, conditions M-R.

Strin- gency Poly- Hybrid Hybridization Wash Con- nucleotide Length Temperature and Temperature dition Hybrid (bp)^(‡) Buffer^(†) and Buffer^(†) A DNA:DNA ≧50 65° C.; 1 × SSC -or- 65° C.; 0.3 × 42° C.; 1 × SSC, 50% SSC formamide B DNA:DNA <50 T_(B)*; 1 × SSC T_(B)*; 1 × SSC C DNA:RNA ≧50 67° C.; 1 × SSC -or- 67° C.; 0.3 × 45° C.; 1 × SSC, 50% SSC formamide D DNA:RNA <50 T_(D)*; 1 × SSC T_(D)*; 1 × SSC E RNA:RNA ≧50 70° C.; 1 × SSC -or- 70° C.; 0.3 × 50° C.; 1 × SSC, 50% SSC formamide F RNA:RNA <50 T_(F)*; 1 × SSC T_(F)*; 1 × SSC G DNA:DNA ≧50 65° C.; 4 × SSC -or- 65° C.; 1 × 42° C.; 4 × SSC, 50% SSC formamide H DNA:DNA <50 T_(H)*; 4 × SSC T_(H)*; 4 × SSC I DNA:RNA ≧50 67° C.; 4 × SSC -or- 67° C.; 1 × 45° C.; 4 × SSC, 50% SSC formamide J DNA:RNA <50 T_(J)*; 4 × SSC T_(J)*; 4 × SSC K RNA:RNA ≧50 70° C.; 4 × SSC -or- 67° C.; 1 × 50° C.; 4 × SSC, 50% SSC formamide L RNA:RNA <50 T_(L)*; 2 × SSC T_(L)*; 2 × SSC M DNA:DNA ≧50 50° C.; 4 × SSC -or- 50° C.; 2 × 40° C.; 6 × SSC, 50% SSC formamide N DNA:DNA <50 T_(N)*; 6 × SSC T_(N)*; 6 × SSC O DNA:RNA ≧50 55° C.; 4 × SSC -or- 55° C.; 2 × 42° C.; 6 × SSC, 50% SSC formamide P DNA:RNA <50 T_(P)*; 6 × SSC T_(P)*; 6 × SSC Q RNA:RNA ≧50 60° C.; 4 × SSC -or- 60° C.; 2 × 45° C.; 6 × SSC, 50% SSC formamide R RNA:RNA <50 T_(R)*; 4 × SSC T_(R)*; 4 × SSC ^(‡)The hybrid length is that anticipated for the hybridized region(s) of the hybridizing polynucleotides. When hybridizing a polynucleotide to a target polynucleotide of unknown sequence, the hybrid length is assumed to be that of the hybridizing polynucleotide. When polynucleotides of known sequence are hybridized, the hybrid length can be determined by aligning the sequences of the polynucleotides and identifying the region or regions of optimal sequence complementarity. ^(†)SSPE (1 × SSPE is 0.15M NaCl, 10 mM NaH₂PO₄, and 1.25 mM EDTA, pH 7.4) can be substituted for SSC (1 × SSC is 0.15M NaCl and 15 mM sodium citrate) in the hybridization and wash buffers; washes are performed for 15 minutes after hybridization is complete. *T_(B)-T_(R): The hybridization temperature for hybrids anticipated to be less than 50 base pairs in length should be 5-10° C. less than the melting temperature (T_(m)) of the hybrid, where T_(m) is determined according to the following equations. For hybrids less than 18 base pairs in length, T_(m)(° C.) = 2(# of A + T bases) + 4(# of G + # C bases). For hybrids between 18 and 49 base pairs in length, T_(m)(° C.) = 81.5 + 16.6(log₁₀[Na⁺]) + 0.41(% G + C) − (600/N), where N is the number of bases in the hybrid, and [Na⁺] is the concentration of sodium ions in the hybridization buffer ([Na⁺] for 1 × SSC = 0.165M).

Additional examples of stringency conditions for polynucleotide hybridization are provided in Sambrook, J., E. F. Fritsch, and T. Maniatis, 1989, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., chapters 9 and 11, and Current Protocols in Molecular Biology, 1995, F. M. Ausubel et al., eds., John Wiley & Sons, Inc., sections 2.10 and 6.3-6.4, incorporated herein by reference.

Preferably, each such hybridizing polynucleotide has a length that is at least 25% (more preferably at least 50%, and most preferably at least 75%) of the length of the polynucleotide of the present invention to which it hybridizes, and has at least 60% sequence identity (more preferably, at least 75% identity; most preferably at least 90% or 95% identity) with the polynucleotide of the present invention to which it hybridizes, where sequence identity is determined by comparing the sequences of the hybridizing polynucleotides when aligned so as to maximize overlap and identity while minimizing sequence gaps.

The isolated polynucleotide endcoing the protein of the invention may be operably linked to an expression control sequence such as the pMT2 or pED expression vectors disclosed in Kaufman et al., Nucleic Acids Res. 19, 4485-4490 (1991), in order to produce the protein recombinantly. Many suitable expression control sequences are known in the art. General methods of expressing recombinant proteins are also known and are exemplified in R. Kaufman, Methods in Enzymology 185, 537-566 (1990). As defined herein “operably linked” means that the isolated polynucleotide of the invention and an expression control sequence are situated within a vector or cell in such a way that the protein is expressed by a host cell which has been transformed (transfected) with the ligated polynucleotide/expression control sequence.

A number of types of cells may act as suitable host cells for expression of the protein. Mammalian host cells include, for example, monkey COS cells, Chinese Hamster Ovary (CHO) cells, human kidney 293 cells, human epidermal A431 cells, human Colo205 cells, 3T3 cells, CV-1 cells, other transformed primate cell lines, normal diploid cells, cell strains derived from in vitro culture of primary tissue, primary explants, HeLa cells, mouse L cells, BHK, HL-60, U937, HaK or Jurkat cells.

Alternatively, it may be possible to produce the protein in lower eukaryotes such as yeast or in prokaryotes such as bacteria. Potentially suitable yeast strains include Saccharomyces cerevisiae, Schizosaccharomyces pombe, Kluyveromyces strains, Candida, or any yeast strain capable of expressing heterologous proteins. Potentially suitable bacterial strains include Escherichia coli, Bacillus subtilis, Salmonella typhimurium, or any bacterial strain capable of expressing heterologous proteins. If the protein is made in yeast or bacteria, it may be necessary to modify the protein produced therein, for example by phosphorylation or glycosylation of the appropriate sites, in order to obtain the functional protein. Such covalent attachments may be accomplished using known chemical or enzymatic methods.

The protein may also be produced by operably linking the isolated polynucleotide of the invention to suitable control sequences in one or more insect expression vectors, and employing an insect expression system. Materials and methods for baculovirus/insect cell expression systems are commercially available in kit form from, e.g., Invitrogen, San Diego, Calif., U.S.A. (the MaxBac® kit), and such methods are well known in the art, as described in Summers and Smith, Texas Agricultural Experiment Station Bulletin No. 1555 (1987) incorporated herein by reference. As used herein, an insect cell capable of expressing a polynucleotide of the present invention is “transformed.”

The protein of the invention may be prepared by culturing transformed host cells under culture conditions suitable to express the recombinant protein. The resulting expressed protein may then be purified from such culture (i.e., from culture medium or cell extracts) using known purification processes, such as gel filtration and ion exchange chromatography. The purification of the protein may also include an affinity column containing agents which will bind to the protein; one or more column steps over such affinity resins as concanavalin A-agarose, heparin-toyopearl® or Cibacrom blue 3GA Sepharose®; one or more steps involving hydrophobic interaction chromatography using such resins as phenyl ether, butyl ether, or propyl ether; or immunoaffinity chromatography.

Alternatively, the protein of the invention may also be expressed in a form which will facilitate purification. For example, it may be expressed as a fusion protein, such as those of maltose binding protein (MBP), glutathione-S-transferase (GST) or thioredoxin (TRX). Kits for expression and purification of such fusion proteins are commercially available from New England BioLabs (Beverly, Mass.), Pharmacia (Piscataway, N.J.) and Invitrogen Corporation (Carlsbad, Calif.), respectively. The protein can also be tagged with an epitope and subsequently purified by using a specific antibody directed to such epitope. One such epitope (“Flag”) is commercially available from the Eastman Kodak Company (New Haven, Conn.).

Finally, one or more reverse-phase high performance liquid chromatography (RP-HPLC) steps employing hydrophobic RP-HPLC media, e.g., silica gel having pendant methyl or other aliphatic groups, can be employed to further purify the protein. Some or all of the foregoing purification steps, in various combinations, can also be employed to provide a substantially homogeneous isolated recombinant protein. The protein thus purified is substantially free of other mammalian proteins and is defined in accordance with the present invention as an “isolated protein.”

The protein of the invention may also be expressed as a product of transgenic animals, e.g., as a component of the milk of transgenic cows, goats, pigs, or sheep which are characterized by somatic or germ cells containing a nucleotide sequence encoding the protein.

The protein may also be produced by known conventional chemical synthesis. Methods for constructing the proteins of the present invention by synthetic means are known to those skilled in the art. The synthetically-constructed protein sequences, by virtue of sharing primary, secondary or tertiary structural and/or conformational characteristics with proteins may possess biological properties in common therewith, including protein activity. Thus, they may be employed as biologically active or immunological substitutes for natural, purified proteins in screening of therapeutic compounds and in immunological processes for the development of antibodies.

The proteins provided herein also include proteins characterized by amino acid sequences similar to those of purified proteins but into which modification are naturally provided or deliberately engineered. For example, modifications in the peptide or DNA sequences can be made by those skilled in the art using known techniques. Modifications of interest in the protein sequences may include the alteration, substitution, replacement, insertion or deletion of a selected amino acid residue in the coding sequence. For example, one or more of the cysteine residues may be deleted or replaced with another amino acid to alter the conformation of the molecule. Techniques for such alteration, substitution, replacement, insertion or deletion are well known to those skilled in the art (see, e.g., U.S. Pat. No. 4,518,584). Preferably, such alteration, substitution, replacement, insertion or deletion retains the desired activity of the protein.

Other fragments and derivatives of the sequences of proteins which would be expected to retain protein activity in whole or in part and may thus be useful for screening or other immunological methodologies may also be easily made by those skilled in the art given the disclosures herein. Such modifications are believed to be encompassed by the present invention.

USES AND BIOLOGICAL ACTIVITY

The polynucleotides and proteins of the present invention are expected to exhibit one or more of the uses or biological activities (including those associated with assays cited herein) identified below. Uses or activities described for proteins of the present invention may be provided by administration or use of such proteins or by administration or use of polynucleotides encoding such proteins (such as, for example, in gene therapies or vectors suitable for introduction of DNA).

Research Uses and Utilities

The polynucleotides provided by the present invention can be used by the research community for various purposes. The polynucleotides can be used to express recombinant protein for analysis, characterization or therapeutic use; as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in disease states); as molecular weight markers on Southern gels; as chromosome markers or tags (when labeled) to identify chromosomes or to map related gene positions; to compare with endogenous DNA sequences in patients to identify potential genetic disorders; as probes to hybridize and thus discover novel, related DNA sequences; as a source of information to derive PCR primers for genetic fingerprinting; as a probe to “subtract-out” known sequences in the process of discovering other novel polynucleotides; for selecting and making oligomers for attachment to a “gene chip” or other support, including for examination of expression patterns; to raise anti-protein antibodies using DNA immunization techniques; and as an antigen to raise anti-DNA antibodies or elicit another immune response. Where the polynucleotide encodes a protein which binds or potentially binds to another protein (such as, for example, in a receptor-ligand interaction), the polynucleotide can also be used in interaction trap assays (such as, for example, those described in Gyuris et al., 1993, Cell 75: 791-803 and in Rossi et al., 1997, Proc. Natl. Acad. Sci. USA 94: 8405-8410, all of which are incorporated by reference herein) to identify polynucleotides encoding the other protein with which binding occurs or to identify inhibitors of the binding interaction.

The proteins provided by the present invention can similarly be used in assay to determine biological activity, including in a panel of multiple proteins for high-throughput screening; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its receptor) in biological fluids; as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state); and, of course, to isolate correlative receptors or ligands. Where the protein binds or potentially binds to another protein (such as, for example, in a receptor-ligand interaction), the protein can be used to identify the other protein with which binding occurs or to identify inhibitors of the binding interaction. Proteins involved in these binding interactions can also be used to screen for peptide or small molecule inhibitors or agonists of the binding interaction.

Any or all of these research utilities are capable of being developed into reagent grade or kit format for commercialization as research products.

Methods for performing the uses listed above are well known to those skilled in the art. References disclosing such methods include without limitation “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds., 1989, and “Methods in Enzymology: Guide to Molecular Cloning Techniques”, Academic Press, Berger, S. L. and A. R. Kimmel eds., 1987.

Nutritional Uses

Polynucleotides and proteins of the present invention can also be used as nutritional sources or supplements. Such uses include without limitation use as a protein or amino acid supplement, use as a carbon source, use as a nitrogen source and use as a source of carbohydrate. In such cases the protein or polynucleotide of the invention can be added to the feed of a particular organism or can be administered as a separate solid or liquid preparation, such as in the form of powder, pills, solutions, suspensions or capsules. In the case of microorganisms, the protein or polynucleotide of the invention can be added to the medium in or on which the microorganism is cultured.

Cytokine and Cell Proliferation/Differentiation Activity

A protein of the present invention may exhibit cytokine, cell proliferation (either inducing or inhibiting) or cell differentiation (either inducing or inhibiting) activity or may induce production of other cytokines in certain cell populations. Many protein factors discovered to date, including all known cytokines, have exhibited activity in one or more factor-dependent cell proliferation assays, and hence the assays serve as a convenient confirmation of cytokine activity. The activity of a protein of the present invention is evidenced by any one of a number of routine factor dependent cell proliferation assays for cell lines including, without limitation, 32D, DA2, DA1G, T10, B9, B9/11, BaF3, MC9/G, M+ (preB M+), 2E8, RB5, DA1, 123, T1165, HT2, CTLL2, TF-1, Mo7e and CMK.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Assays for T-cell or thymocyte proliferation include without limitation those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 3, In Vitro assays for Mouse Lymphocyte Function 3.1-3.19; Chapter 7, Immunologic studies in Humans); Takai et al., J. Immunol. 137:3494-3500, 1986; Bertagnolli et al., J. Immunol. 145:1706-1712, 1990; Bertagnolli et al., Cellular Immunology 133:327-341, 1991; Bertagnolli, et al., J. Immunol. 149:3778-3783, 1992; Bowman et al., J. Immunol. 152: 1756-1761, 1994.

Assays for cytokine production and/or proliferation of spleen cells, lymph node cells or thymocytes include, without limitation, those described in: Polyclonal T cell stimulation, Kruisbeek, A. M. and Shevach, E. M. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 3.12.1-3.12.14, John Wiley and Sons, Toronto. 1994; and Measurement of mouse and human Interferon γ, Schreiber, R. D. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 6.8.1-6.8.8, John Wiley and Sons, Toronto. 1994.

Assays for proliferation and differentiation of hematopoietic and lymphopoietic cells include, without limitation, those described in: Measurement of Human and Murine Interleukin 2 and Interleukin 4, Bottomly, K., Davis, L. S. and Lipsky, P. E. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 6.3.1-6.3.12, John Wiley and Sons, Toronto. 1991; deVries et al., J. Exp. Med. 173:1205-1211, 1991; Moreau et al., Nature 336:690-692, 1988; Greenberger et al., Proc. Natl. Acad. Sci. U.S.A. 80:2931-2938, 1983; Measurement of mouse and human interleukin 6—Nordan, R. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 6.6.1-6.6.5, John Wiley and Sons, Toronto. 1991; Smith et al., Proc. Natl. Acad. Sci. U.S.A. 83:1857-1861, 1986; Measurement of human Interleukin 11—Bennett, F., Giannotti, J., Clark, S. C. and Turner, K. J. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 6.15.1 John Wiley and Sons, Toronto. 1991; Measurement of mouse and human Interleukin 9—Ciarletta, A., Giannotti, J., Clark, S. C. and Turner, K. J. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 6.13.1, John Wiley and Sons, Toronto. 1991.

Assays for T-cell clone responses to antigens (which will identify, among others, proteins that affect APC-T cell interactions as well as direct T-cell effects by measuring proliferation and cytokine production) include, without limitation, those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 3, In Vitro assays for Mouse Lymphocyte Function; Chapter 6, Cytokines and their cellular receptors; Chapter 7, Immunologic studies in Humans); Weinberger et al., Proc. Natl. Acad. Sci. USA 77:6091-6095, 1980; Weinberger et al., Eur. J. Immun. 11:405-411, 1981; Takai et al., J. Immunol. 137:3494-3500, 1986; Takai et al., J. Immunol. 140:508-512, 1988.

Immune Stimulating or Suppressing Activity

A protein of the present invention may also exhibit immune stimulating or immune suppressing activity, including without limitation the activities for which assays are described herein. A protein may be useful in the treatment of various immune deficiencies and disorders (including severe combined immunodeficiency (SCID)), e.g., in regulating (up or down) growth and proliferation of T and/or B lymphocytes, as well as effecting the cytolytic activity of NK cells and other cell populations. These immune deficiencies may be genetic or be caused by viral (e.g., HIV) as well as bacterial or fungal infections, or may result from autoimmune disorders. More specifically, infectious diseases causes by viral, bacterial, fungal or other infection may be treatable using a protein of the present invention, including infections by HIV, hepatitis viruses, herpesviruses, mycobacteria, Leishmania spp., malaria spp. and various fungal infections such as candidiasis. Of course, in this regard, a protein of the present invention may also be useful where a boost to the immune system generally may be desirable, i.e., in the treatment of cancer.

Autoimmune disorders which may be treated using a protein of the present invention include, for example, connective tissue disease, multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, autoimmune pulmonary inflammation, Guillain-Barre syndrome, autoimmune thyroiditis, insulin dependent diabetes mellitis, myasthenia gravis, graft-versus-host disease and autoimmune inflammatory eye disease. Such a protein of the present invention may also to be useful in the treatment of allergic reactions and conditions, such as asthma (particularly allergic asthma) or other respiratory problems. Other conditions, in which immune suppression is desired (including, for example, organ transplantation), may also be treatable using a protein of the present invention.

Using the proteins of the invention it may also be possible to regulate immune responses in a number of ways. Down regulation may be in the form of inhibiting or blocking an immune response already in progress or may involve preventing the induction of an immune response. The functions of activated T cells may be inhibited by suppressing T cell responses or by inducing specific tolerance in T cells, or both. Immunosuppression of T cell responses is generally an active, non-antigen-specific, process which requires continuous exposure of the T cells to the suppressive agent. Tolerance, which involves inducing non-responsiveness or energy in T cells, is distinguishable from immunosuppression in that it is generally antigen-specific and persists after exposure to the tolerizing agent has ceased. Operationally, tolerance can be demonstrated by the lack of a T cell response upon reexposure to specific antigen in the absence of the tolerizing agent.

Down regulating or preventing one or more antigen functions (including without limitation B lymphocyte antigen functions (such as, for example, B7)), e.g., preventing high level lymphokine synthesis by activated T cells, will be useful in situations of tissue, skin and organ transplantation and in graft-versus-host disease (GVHD). For example, blockage of T cell function should result in reduced tissue destruction in tissue transplantation. Typically, in tissue transplants, rejection of the transplant is initiated through its recognition as foreign by T cells, followed by an immune reaction that destroys the transplant. The administration of a molecule which inhibits or blocks interaction of a B7 lymphocyte antigen with its natural ligand(s) on immune cells (such as a soluble, monomeric form of a peptide having B7-2 activity alone or in conjunction with a monomeric form of a peptide having an activity of another B lymphocyte antigen (e.g., B7-1, B7-3) or blocking antibody), prior to transplantation can lead to the binding of the molecule to the natural ligand(s) on the immune cells without transmitting the corresponding costimulatory signal. Blocking B lymphocyte antigen function in this matter prevents cytokine synthesis by immune cells, such as T cells, and thus acts as an immunosuppressant. Moreover, the lack of costimulation may also be sufficient to anergize the T cells, thereby inducing tolerance in a subject. Induction of long-term tolerance by B lymphocyte antigen-blocking reagents may avoid the necessity of repeated administration of these blocking reagents. To achieve sufficient immunosuppression or tolerance in a subject, it may also be necessary to block the function of a combination of B lymphocyte antigens.

The efficacy of particular blocking reagents in preventing organ transplant rejection or GVHD can be assessed using animal models that are predictive of efficacy in humans. Examples of appropriate systems which can be used include allogeneic cardiac grafts in rats and xenogeneic pancreatic islet cell grafts in mice, both of which have been used to examine the immunosuppressive effects of CTLA4Ig fusion proteins in vivo as described in Lenschow et al., Science 257:789-792 (1992) and Turka et al., Proc. Natl. Acad. Sci USA, 89:11102-11105 (1992). In addition, murine models of GVHD (see Paul ed., Fundamental Immunology, Raven Press, New York, 1989, pp. 846-847) can be used to determine the effect of blocking B lymphocyte antigen function in vivo on the development of that disease.

Blocking antigen function may also be therapeutically useful for treating autoimmune diseases. Many autoimmune disorders are the result of inappropriate activation of T cells that are reactive against self tissue and which promote the production of cytokines and autoantibodies involved in the pathology of the diseases. Preventing the activation of autoreactive T cells may reduce or eliminate disease symptoms. Administration of reagents which block costimulation of T cells by disrupting receptor:ligand interactions of B lymphocyte antigens can be used to inhibit T cell activation and prevent production of autoantibodies or T cell-derived cytokines which may be involved in the disease process. Additionally, blocking reagents may induce antigen-specific tolerance of autoreactive T cells which could lead to long-term relief from the disease. The efficacy of blocking reagents in preventing or alleviating autoimmune disorders can be determined using a number of well-characterized animal models of. human autoimmune diseases. Examples include murine experimental autoimmune encephalitis, systemic lupus erythmatosis in MRL/lpr/lpr mice or NZB hybrid mice, murine autoimmune collagen arthritis, diabetes mellitus in NOD mice and BB rats, and murine experimental myasthenia gravis (see Paul ed., Fundamental Immunology, Raven Press, New York, 1989, pp. 840-856).

Upregulation of an antigen function (preferably a B lymphocyte antigen function), as a means of up regulating immune responses, may also be useful in therapy. Upregulation of immune responses may be in the form of enhancing an existing immune response or eliciting an initial immune response. For example, enhancing an immune response through stimulating B lymphocyte antigen function may be useful in cases of viral infection. In addition, systemic viral diseases such as influenza, the common cold, and encephalitis might be alleviated by the administration of stimulatory forms of B lymphocyte antigens systemically.

Alternatively, anti-viral immune responses may be enhanced in an infected patient by removing T cells from the patient, costimulating the T cells in vitro with viral antigen-pulsed APCs either expressing a peptide of the present invention or together with a stimulatory form of a soluble peptide of the present invention and reintroducing the in vitro activated T cells into the patient. Another method of enhancing anti-viral immune responses would be to isolate infected cells from a patient, transfect them with a nucleic acid encoding a protein of the present invention as described herein such that the cells express all or a portion of the protein on their surface, and reintroduce the transfected cells into the patient. The infected cells would now be capable of delivering a costimulatory signal to, and thereby activate, T cells in vivo.

In another application, up regulation or enhancement of antigen function (preferably B lymphocyte antigen function) may be useful in the induction of. tumor immunity. Tumor cells (e.g., sarcoma, melanoma, lymphoma, leukemia, neuroblastoma, carcinoma) transfected with a nucleic acid encoding at least one peptide of the present invention can be administered to a subject to overcome tumor-specific tolerance in the subject. If desired, the tumor cell can be transfected to express a combination of peptides. For example, tumor cells obtained from a patient can be transfected ex vivo with an expression vector directing the expression of a peptide having B7-2-like activity alone, or in conjunction with a peptide having B7-1-like activity and/or B7-3-like activity. The transfected tumor cells are returned to the patient to result in expression of the peptides on the surface of the transfected cell. Alternatively, gene therapy techniques can be used to target a tumor cell for transfection in vivo.

The presence of the peptide of the present invention having the activity of a B lymphocyte antigen(s) on the surface of the tumor cell provides the necessary costimulation signal to T cells to induce a T cell mediated immune response against the transfected tumor cells. In addition, tumor cells which lack MHC class I or MHC class II molecules, or which fail to reexpress sufficient amounts of MHC class I or MHC class II molecules, can be transfected with nucleic acid encoding all or a portion of (e.g., a cytoplasmic-domain truncated portion) of an MHC class I α chain protein and β₂ microglobulin protein or an MHC class II α chain protein and an MHC class II β chain protein to thereby express MHC class I or MHC class II proteins on the cell surface. Expression of the appropriate class I or class II MHC in conjunction with a peptide having the activity of a B lymphocyte antigen (e.g., B7-1, B7-2, B7-3) induces a T cell mediated immune response against the transfected tumor cell. Optionally, a gene encoding an antisense construct which blocks expression of an MHC class II associated protein, such as the invariant chain, can also be cotransfected with a DNA encoding a peptide having the activity of a B lymphocyte antigen to promote presentation of tumor associated antigens and induce tumor specific immunity. Thus, the induction of a T cell mediated immune response in a human subject may be sufficient to overcome tumor-specific tolerance in the subject.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Suitable assays for thymocyte or splenocyte cytotoxicity include, without limitation, those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 3, In Vitro assays for Mouse Lymphocyte Function 3.1-3.19; Chapter 7, Immunologic studies in Humans); Herrmann et al., Proc. Natl. Acad. Sci. USA 78:2488-2492, 1981; Herrmann et al., J. Immunol. 128:1968-1974, 1982; Handa et al., J. Immunol. 135:1564-1572, 1985; Takai et al., J. Immunol. 137:3494-3500, 1986; Takai et al., J. Immunol. 140:508-512, 1988; Herrmann et al., Proc. Natl. Acad. Sci. USA 78:2488-2492, 1981; Herrmann et al., J. Immunol. 128:1968-1974, 1982; Handa et al., J. Immunol. 135:1564-1572, 1985; Takai et al., J. Immunol. 137:3494-3500, 1986; Bowmanet al., J. Virology 61:1992-1998; Takai et al., J. Immunol. 140:508-512, 1988; Bertagnolr et al., Cellular Immunology 133:327-341, 1991; Brown et al., J. Immunol. 153:3079-3092, 1994.

Assays for T-cell-dependent immunoglobulin responses and isotype switching (which will identify, among others, proteins that modulate T-cell dependent antibody responses and that affect Th1/Th2 profiles) include, without limitation, those described in: Maliszewski, J. Immunol. 144:3028-3033, 1990; and Assays for B cell function: In vitro antibody production, Mond, J. J. and Brunswick, M. In Current Protocols in Immunology. J. E. e.a. Coligan eds. Vol 1 pp. 3.8.1-3.8.16, John Wiley and Sons, Toronto. 1994.

Mixed lymphocyte reaction (MLR) assays (which will identify, among others, proteins that generate predominantly Th1 and CTL responses) include, without limitation, those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 3, In Vitro assays for Mouse Lymphocyte Function 3.1-3.19; Chapter 7, Immunologic studies in Humans); Takai et al., J. Immunol. 137:3494-3500, 1986; Takai et al., J. Immunol. 140:508-512, 1988; Bertagnolli et al., J. Immunol. 149:3778-3783, 1992.

Dendritic cell-dependent assays (which will identify, among others, proteins expressed by dendritic cells that activate naive T-cells) include, without limitation, those described in: Guery et al., J. Immunol. 134:536-544, 1995; Inaba et al., Journal of Experimental Medicine 173:549-559, 1991; Macatonia et al., Journal of Immunology 154:5071-5079, 1995; Porgador et al., Journal of Experimental Medicine 182:255-260, 1995; Nair et al., Journal of Virology 67:4062-4069, 1993; Huang et al., Science 264:961-965, 1994; Macatonia et al., Journal of Experimental Medicine 169:1255-1264, 1989; Bhardwaj et al., Journal of Clinical Investigation 94:797-807, 1994; and Inaba et al., Journal of Experimental Medicine 172:631-640, 1990.

Assays for lymphocyte survival/apoptosis (which will identify, among others, proteins that prevent apoptosis after superantigen induction and proteins that regulate lymphocyte homeostasis) include, without limitation, those described in: Darzynkiewicz et al., Cytometry 13:795-808, 1992; Gorczyca et al., Leukemia 7:659-670, 1993; Gorczyca et al., Cancer Research 53:1945-1951, 1993; Itoh et al., Cell 66:233-243, 1991; Zacharchuk, Journal of Immunology 145:4037-4045, 1990; Zamai et al., Cytometry 14:891-897, 1993; Gorczyca et al., International Journal of Oncology 1:639-648, 1992.

Assays for proteins that influence early steps of T-cell commitment and development include, without limitation, those described in: Antica et al., Blood 84:111-117, 1994; Fine et al., Cellular Immunology 155:111-122, 1994; Galy et al., Blood 85:2770-2778, 1995; Toki et al., Proc. Nat. Acad Sci. USA 88:7548-7551, 1991.

Hematopoiesis Regulating Activity

A protein of the present invention may be useful in regulation of hematopoiesis and, consequently, in the treatment of myeloid or lymphoid cell deficiencies. Even marginal biological activity in support of colony forming cells or of factor-dependent cell lines indicates involvement in regulating hematopoiesis, e.g. in supporting the growth and proliferation of erythroid progenitor cells alone or in combination with other cytokines, thereby indicating utility, for example, in treating various anemias or for use in conjunction with irradiation/chemotherapy to stimulate the production of erythroid precursors and/or erythroid cells; in supporting the growth and proliferation of myeloid cells such as granulocytes and monocytes/macrophages (i.e., traditional CSF activity) useful, for example, in conjunction with chemotherapy to prevent or treat consequent myelo-suppression; in supporting the growth and proliferation of megakaryocytes and consequently of platelets thereby allowing prevention or treatment of various platelet disorders such as thrombocytopenia, and generally for use in place of or complimentary to platelet transfusions; and/or in supporting the growth and proliferation of hematopoietic stem cells which are capable of maturing to any and all of the above-mentioned hematopoietic cells and therefore find therapeutic utility in various stem cell disorders (such as those usually treated with transplantation, including, without limitation, aplastic anemia and paroxysmal nocturnal hemoglobinuria), as well as in repopulating the stem cell compartment post irradiation/chemotherapy, either in-vivo or ex-vivo (i.e., in conjunction with bone marrow transplantation or with peripheral progenitor cell transplantation (homologous or heterologous)) as normal cells or genetically manipulated for gene therapy.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Suitable assays for proliferation and differentiation of various hematopoietic lines are cited above.

Assays for embryonic stem cell differentiation (which will identify; among others, proteins that influence embryonic differentiation hematopoiesis) include, without limitation, those described in: Johansson et al. Cellular Biology 15:141-151, 1995; Keller et al., Molecular and Cellular Biology 13:473486, 1993; McClanahan et al., Blood 81:2903-2915, 1993.

Assays for stem cell survival and differentiation (which will identify, among others, proteins that regulate lympho-hematopoiesis) include, without limitation, those described in: Methylcellulose colony forming assays, Freshney, M. G. In Culture of Hematopoietic Cells. R. I. Freshney, et al. eds. Vol pp. 265-268, Wiley-Liss, Inc., New York, N.Y. 1994; Hirayama et al., Proc. Natl. Acad. Sci. USA 89:5907-5911, 1992; Primitive hematopoietic colony forming cells with high proliferative potential, McNiece, I. K. and Briddell, R. A. In Culture of Hematopoietic Cells. R. I. Freshney, et al. eds. Vol pp. 23-39, Wiley-Liss, Inc., New York, N.Y. 1994; Neben et al., Experimental Hematology 22:353-359, 1994; Cobblestone area forming cell assay, Ploemacher, R. E. In Culture of Hematopoietic Cells. R. I. Freshney, et al. eds. Vol pp. 1-21, Wiley-Liss, Inc., New York, N.Y. 1994; Long term bone marrow cultures in the presence of stromal cells, Spooncer, E., Dexter, M. and Allen, T. In Culture of Hematopoietic Cells. R. I. Freshney, et al. eds. Vol pp. 163-179, Wiley-Liss, Inc., New York, N.Y. 1994; Long term culture initiating cell assay, Sutherland, H. J. In Culture of Hematopoietic Cells. R. I. Freshney, et al. eds. Vol pp. 139-162, Wiley-Liss, Inc., New York, N.Y. 1994.

Tissue Growth Activity

A protein of the present invention also may have utility in compositions used for bone, cartilage, tendon, ligament and/or nerve tissue growth or regeneration, as well as for wound healing and tissue repair and replacement, and in the treatment of burns, incisions and ulcers.

A protein of the present invention, which induces cartilage and/or bone growth in circumstances where bone is not normally formed, has application in the healing of bone fractures and cartilage damage or defects in humans and other animals. Such a preparation employing a protein of the invention may have prophylactic use in closed as well as open fracture reduction and also in the improved fixation of artificial joints. De novo bone formation induced by an osteogenic agent contributes to the repair of congenital, trauma induced, or oncologic resection induced craniofacial defects, and also is useful in cosmetic plastic surgery.

A protein of this invention may also be used in the treatment of periodontal disease, and in other tooth repair processes. Such agents may provide an environment to attract bone-forming cells, stimulate growth of bone-forming cells -or induce differentiation of progenitors of bone-forming cells. A protein of the invention may also be useful in the treatment of osteoporosis or osteoarthritis, such as through stimulation of bone and/or cartilage repair or by blocking inflammation or processes of tissue destruction (collagenase activity, osteoclast activity, etc.) mediated by inflammatory processes.

Another category of tissue regeneration activity that may be attributable to the protein of the present invention is tendon/ligament formation. A protein of the present invention, which induces tendon/ligament-like tissue or other tissue formation in circumstances where such tissue is not normally formed, has application in the healing of tendon or ligament tears, deformities and other tendon or ligament defects in humans and other animals. Such a preparation employing a tendon/ligament-like tissue inducing protein may have prophylactic use in preventing damage to tendon or ligament tissue, as well as use in the improved fixation of tendon or ligament to bone or other tissues, and in repairing defects to tendon or ligament tissue. De novo tendon/ligament-like tissue formation induced by a composition of the present invention contributes to the repair of congenital, trauma induced, or other tendon or ligament defects of other origin, and is also useful in cosmetic plastic surgery for attachment or repair of tendons or ligaments. The compositions of the present invention may provide an environment to attract tendon- or ligament-forming cells, stimulate growth of tendon- or ligament-forming cells, induce differentiation of progenitors of tendon- or ligament-forming cells, or induce growth of tendon/ligament cells or progenitors ex vivo for return in vivo to effect tissue repair. The compositions of the invention may also be useful in the treatment of tendinitis, carpal tunnel syndrome and other tendon or ligament defects. The compositions may also include an appropriate matrix and/or sequestering agent as a carrier as is well known in the art.

The protein of the present invention may also be useful for proliferation of neural cells and for regeneration of nerve and brain tissue, i.e. for the treatment of central and peripheral nervous system diseases and neuropathies, as well as mechanical and traumatic disorders, which involve degeneration, death or trauma to neural cells or nerve tissue. More specifically, a protein may be used in the treatment of diseases of the peripheral nervous system, such as peripheral nerve injuries, peripheral neuropathy and localized neuropathies, and central nervous system diseases, such as Alzheimer's, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Shy-Drager syndrome. Further conditions which may be treated in accordance with the present invention include mechanical and traumatic disorders, such as spinal cord disorders, head trauma and cerebrovascular diseases such as stroke. Peripheral neuropathies resulting from chemotherapy or other medical therapies may also be treatable using a protein of the invention.

Proteins of the invention may also be useful to promote better or faster closure of non-healing wounds, including without limitation pressure ulcers, ulcers associated with vascular insufficiency, surgical and traumatic wounds, and the like.

It is expected that a protein of the present invention may also exhibit activity for generation or regeneration of other tissues, such as organs (including, for example, pancreas, liver, intestine, kidney, skin, endothelium), muscle (smooth, skeletal or cardiac) and vascular (including vascular endothelium) tissue, or for promoting the growth of cells comprising such tissues. Part of the desired effects may be by inhibition or modulation of fibrotic scarring to allow normal tissue to regenerate. A protein of the invention may also exhibit angiogenic activity.

A protein of the present invention may also be useful for gut protection or regeneration and treatment of lung or liver fibrosis, reperfusion injury in various tissues, and conditions resulting from systemic cytokine damage.

A protein of the present invention may also be useful for promoting or inhibiting differentiation of tissues described above from precursor tissues or cells; or for inhibiting the growth of tissues described above.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Assays for tissue generation activity include, without limitation, those described in: International Patent Publication No. WO95/16035 (bone, cartilage, tendon); International Patent Publication No. WO95/05846 (nerve, neuronal); International Patent Publication No. WO91/07491 (skin, endothelium).

Assays for wound healing activity include, without limitation, those described in: Winter, Epidermal Wound Healing pps. 71-112 (Maibach, H I and Rovee, D T, eds.), Year Book Medical Publishers, Inc., Chicago, as modified by Eaglstein and Mertz, J. Invest. Dermatol 71:382-84 (1978).

Activin/Inhibin Activity

A protein of the present invention may also exhibit activin- or inhibin-related activities. Inhibins are characterized by their ability to inhibit the release of follicle stimulating hormone (FSH), while activins and are characterized by their ability to stimulate the release of follicle stimulating hormone (FSH). Thus, a protein of the present invention, alone or in heterodimers with a member of the inhibin a family, may be useful as a contraceptive based on the ability of inhibins to decrease fertility in female mammals and decrease spermatogenesis in male mammals. Administration of sufficient amounts of other inhibins can induce infertility in these mammals. Alternatively, the protein of the invention, as a homodimer or as a heterodimer with other protein subunits of the inhibin-β group, may be useful as a fertility inducing therapeutic, based upon the ability of activin molecules in stimulating FSH release from cells of the anterior pituitary. See, for example, U.S. Pat. No. 4,798,885. A protein of the invention may also be useful for advancement of the onset of fertility in sexually immature mammals, so as to increase the lifetime reproductive performance of domestic animals such as cows, sheep and pigs.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Assays for activin/inhibin activity include, without limitation, those described in: Vale et al., Endocrinology 91:562-572, 1972; Ling et al., Nature 321:779-782, 1986; Vale et al., Nature 321:776-779, 1986; Mason et al., Nature 318:659-663, 1985; Forage et al., Proc. Natl. Acad. Sci. USA 83:3091-3095, 1986.

Chemotactic/Chemokinetic Activity

A protein of the present invention may have chemotactic or chemokinetic activity (e.g., act as a chemokine) for mammalian cells, including, for example, monocytes, fibroblasts, neutrophils, T-cells, mast cells, eosinophils, epithelial and/or endothelial cells. Chemotactic and chemokinetic proteins can be used to mobilize or attract a desired cell population to a desired site of action. Chemotactic or chemokinetic proteins provide particular advantages in treatment of wounds and other trauma to tissues, as well as in treatment of localized infections. For example, attraction of lymphocytes, monocytes or neutrophils to tumors or sites of infection may result in improved immune responses against the tumor or infecting agent.

A protein or peptide has chemotactic activity for a particular cell population if it can stimulate, directly or indirectly, the directed orientation or movement of such cell population. Preferably, the protein or peptide has the ability to directly stimulate directed movement of cells. Whether a particular protein has chemotactic activity for a population of cells can be readily determined by employing such protein or peptide in any known assay for cell chemotaxis.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Assays for chemotactic activity (which will identify proteins that induce or prevent chemotaxis) consist of assays that measure the ability of a protein to induce the migration of cells across a membrane as well as the ability of a protein to induce the adhesion of one cell population to another cell population. Suitable assays for movement and adhesion include, without limitation, those described in: Current Protocols in Immunology, Ed by J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W. Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 6.12, Measurement of alpha and beta Chemokines 6.12.1-6.12.28; Taub et al. J. Clin. Invest. 95:1370-1376, 1995; Lind et al. APMIS 103:140-146, 1995; Muller et al Eur. J. Immunol. 25: 1744_(—)1748; Gruber et al. J. of Immunol. 152:5860-5867, 1994; Johnston et al. J. of Immunol. 153: 1762-1768, 1994.

Hemostatic and Thrombolytic Activity

A protein of the invention may also exhibit hemostatic or thrombolytic activity. As a result, such a protein is expected to be useful in treatment of various coagulation disorders (including hereditary disorders, such as hemophilias) or to enhance coagulation and other hemostatic events in treating wounds resulting from trauma, surgery or other causes. A protein of the invention may also be useful for dissolving or inhibiting formation of thromboses and for treatment and prevention of conditions resulting therefrom (such as, for example, infarction of cardiac and central nervous system vessels (e.g., stroke).

The activity of a protein of the invention may, among other means, be measured by the following methods:

Assay for hemostatic and thrombolytic activity include, without limitation, those described in: Linet et al., J. Clin. Pharmacol. 26:131-140, 1986; Burdick et al., Thrombosis Res. 45:413-419, 1987; Humphrey et al., Fibrinolysis 5:71-79 (1991); Schaub, Prostaglandins 35:467-474, 1988.

Receptor/Ligand Activity

A protein of the present invention may also demonstrate activity as receptors, receptor ligands or inhibitors or agonists of receptor/ligand interactions. Examples of such receptors and ligands include, without limitation, cytokine receptors and their ligands, receptor kinases and their ligands, receptor phosphatases and their ligands, receptors involved in cell-cell interactions and their ligands (including without limitation, cellular adhesion molecules (such as selectins, integrins and their ligands) and receptor/ligand pairs involved in antigen presentation, antigen recognition and development of cellular and humoral immune responses). Receptors and ligands are also useful for screening of potential peptide or small molecule inhibitors of the relevant receptor/ligand interaction. A protein of the present invention (including, without limitation, fragments of receptors and ligands) may themselves be useful as inhibitors of receptor/ligand interactions.

The activity of a protein of the invention may, among other means, be measured by the following methods:

Suitable assays for receptor-ligand activity include without limitation those described in:Current Protocols in Immunology, Ed by J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W. Strober, Pub. Greene Publishing Associates and Wiley-Interscience (Chapter 7.28, Measurement of Cellular Adhesion under static conditions 7.28.1-7.28.22), Takai et al., Proc. Natl. Acad. Sci. USA 84:6864-6868, 1987; Bierer et al., J. Exp. Med. 168:1145-1156, 1988; Rosenstein et al., J. Exp. Med. 169:149-160 1989; Stoltenborg et al., J. Immunol. Methods 175:59-68, 1994; Stitt et al., Cell 80:661-670, 1995.

Anti-inflammatory Activity

Proteins of the present invention may also exhibit anti-inflammatory activity. The anti-inflammatory activity may be achieved by providing a stimulus to cells involved in the inflammatory response, by inhibiting or promoting cell-cell interactions (such as, for example, cell adhesion), by inhibiting or promoting chemotaxis of cells involved in the inflammatory process, inhibiting or promoting cell extravasation, or by stimulating or suppressing production of other factors which more directly inhibit or promote an inflammatory response. Proteins exhibiting such activities can be used to treat inflammatory conditions including chronic or acute conditions), including without limitation inflammation associated with infection (such as septic shock, sepsis or systemic inflammatory response syndrome (SIRS)), ischemia-reperfusion injury, endotoxin lethality, arthritis, complement-mediated hyperacute rejection, nephritis, cytokine or chemokine-induced lung injury, inflammatory bowel disease, Crohn's disease or resulting from over production of cytokines such as TNF or IL-1. Proteins of the invention may also be useful to treat anaphylaxis and hypersensitivity to an antigenic substance or material.

Cadherin/Tumor Invasion Suppressor Activity

Cadherins are calcium-dependent adhesion molecules that appear to play major roles during development, particularly in defining specific cell types. Loss or alteration of normal cadherin expression can lead to changes in cell adhesion properties linked to tumor growth and metastasis. Cadherin malfunction is also implicated in other human diseases, such as pemphigus vulgaris and pemphigus foliaceus (auto-immune blistering skin diseases), Crohn's disease, and some developmental abnormalities.

The cadherin superfamily includes well over forty members, each with a distinct pattern of expression. All members of the superfamily have in common conserved extracellular repeats (cadherin domains), but structural differences are found in other parts of the molecule. The cadherin domains bind calcium to form their tertiary structure and thus calcium is required to mediate their adhesion. Only a few amino acids in the first cadherin domain provide the basis for homophilic adhesion; modification of this recognition site can change the specificity of a cadherin so that instead of recognizing only itself, the mutant molecule can now also bind to a different cadherin. In addition, some cadherins engage in heterophilic adhesion with other cadherins.

E-cadherin, one member of the cadherin superfamily, is expressed in epithelial cell types. Pathologically, if E-cadherin expression is lost in a tumor, the malignant cells become invasive and the cancer metastasizes. Transfection of cancer cell lines with polynucleotides expressing E-cadherin has reversed cancer-associated changes by returning altered cell shapes to normal, restoring cells' adhesiveness to each other and to their substrate, decreasing the cell growth rate, and drastically reducing anchorage-independent cell growth. Thus, reintroducing E-cadherin expression reverts carcinomas to a less advanced stage. It is likely that other cadherins have the same invasion suppressor role in carcinomas derived from other tissue types. Therefore, proteins of the present invention with cadherin activity, and polynucleotides of the present invention encoding such proteins, can be used to treat cancer. Introducing such proteins or polynucleotides into cancer cells can reduce or eliminate the cancerous changes observed in these cells by providing normal cadherin expression.

Cancer cells have also been shown to express cadherins of a different tissue type than their origin, thus allowing these cells to invade and metastasize in a different tissue in the body. Proteins of the present invention with cadherin activity, and polynucleotides of the present invention encoding such proteins, can be substituted in these cells for the inappropriately expressed cadherins, restoring normal cell adhesive properties and reducing or eliminating the tendency of the cells to metastasize.

Additionally, proteins of the present invention with cadherin activity, and polynucleotides of the present invention encoding such proteins, can used to generate antibodies recognizing and binding to cadherins. Such antibodies can be used to block the adhesion of inappropriately expressed tumor-cell cadherins, preventing the cells from forming a tumor elsewhere. Such an anti-cadherin antibody can also be used as a marker for the grade, pathological type, and prognosis of a cancer, i.e. the more progressed the cancer, the less cadherin expression there will be, and this decrease in cadherin expression can be detected by the use of a cadherin-binding antibody.

Fragments of proteins of the present invention with cadherin activity, preferably a polypeptide comprising a decapeptide of the cadherin recognition site, and polynucleotides of the present invention encoding such protein fragments, can also be used to block cadherin function by binding to cadherins and preventing them from binding in ways that produce undesirable effects. Additionally, fragments of proteins of the present invention with cadherin activity, preferably truncated soluble cadherin fragments which have been found to be stable in the circulation of cancer patients, and polynucleotides encoding such protein fragments, can be used to disturb proper cell-cell adhesion.

Assays for cadherin adhesive and invasive suppressor activity include, without limitation, those described in: Hortsch et al. J Biol Chem 270 (32): 18809-18817, 1995; Miyaki et al. Oncogene 11: 2547-2552, 1995; Ozawa et al. Cell 63: 1033-1038, 1990.

Tumor Inhibition Activity

In addition to the activities described above for immunological treatment or prevention of tumors, a protein of the invention may exhibit other anti-tumor activities. A protein may inhibit tumor growth directly or indirectly (such as, for example, via antibody-dependent cell-mediated cytotoxicity (ADCC)). A protein may exhibit its tumor inhibitory activity by acting on tumor tissue or tumor precursor tissue, by inhibiting formation of tissues necessary to support tumor growth (such as, for example, by inhibiting angiogenesis), by causing production of other factors, agents or cell types which inhibit tumor growth, or by suppressing, eliminating or inhibiting factors, agents or cell types which promote tumor growth.

Other Activities

A protein of the invention may also exhibit one or more of the following additional activities or effects: inhibiting the growth, infection or function of, or killing, infectious agents, including, without limitation, bacteria, viruses, fungi and other parasites; effecting (suppressing or enhancing) bodily characteristics, including, without limitation, height, weight, hair color, eye color, skin, fat to lean ratio or other tissue pigmentation, or organ or body part size or shape (such as, for example, breast augmentation or diminution, change in bone form or shape); effecting biorhythms or caricadic cycles or rhythms; effecting the fertility of male or female subjects; effecting the metabolism, catabolism, anabolism, processing, utilization, storage or elimination of dietary fat, lipid, protein, carbohydrate, vitamins, minerals, cofactors or other nutritional factors or component(s); effecting behavioral characteristics, including, without limitation, appetite, libido, stress, cognition (including cognitive disorders), depression (including depressive disorders) and violent behaviors; providing analgesic effects or other pain reducing effects; promoting differentiation and growth of embryonic stem cells in lineages other than hematopoietic lineages; hormonal or endocrine activity; in the case of enzymes, correcting deficiencies of the enzyme and treating deficiency-related diseases; treatment of hyperproliferative disorders (such as, for example, psoriasis); immunoglobulin-like activity (such as, for example, the ability to bind antigens or complement); and the ability to act as an antigen in a vaccine composition to raise an immune response against such protein or another material or entity which is cross-reactive with such protein.

ADMINISTRATION AND DOSING

A protein of the present invention (from whatever source derived, including without limitation from recombinant and non-recombinant sources) may be used in a pharmaceutical composition when combined with a pharmaceutically acceptable carrier.

Such a composition may also contain (in addition to protein and a carrier) diluents, fillers, salts, buffers, stabilizers, solubilizers, and other materials well known in the art. The term “pharmaceutically acceptable” means a non-toxic material that does not interfere with the effectiveness of the biological activity of the active ingredient(s). The characteristics of the carrier will depend on the route of administration. The pharmaceutical composition of the invention may also contain cytokines, lymphokines, or other hematopoietic factors such as M-CSF, GM-CSF, TNF, IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IFN, TNF0, TNF1, TNF2, G-CSF, Meg-CSF, thrombopoietin, stem cell factor, and erythropoietin. The pharmaceutical composition may further contain other agents which either enhance the activity of the protein or compliment its activity or use in treatment. Such additional factors and/or agents may be included in the pharmaceutical composition to produce a synergistic effect with protein of the invention, or to minimize side effects. Conversely, protein of the present invention may be included in formulations of the particular cytokine, lymphokine, other hematopoietic factor, thrombolytic or anti-thrombotic factor, or anti-inflammatory agent to minimize side effects of the cytokine, lymphokine, other hematopoietic factor, thrombolytic or anti-thrombotic factor, or anti-inflammatory agent.

A protein of the present invention may be active in multimers (e.g., heterodimers or homodimers) or complexes with itself or other proteins. As a result, pharmaceutical compositions of the invention may comprise a protein of the invention in such multimeric or complexed form.

The pharmaceutical composition of the invention may be in the form of a complex of the protein(s) of present invention along with protein or peptide antigens. The protein and/or peptide antigen will deliver a stimulatory signal to both B and T lymphocytes. B lymphocytes will respond to antigen through their surface immunoglobulin receptor. T lymphocytes will respond to antigen through the T cell receptor (TCR) following presentation of the antigen by MHC proteins. MHC and structurally related proteins including those encoded by class I and class II MHC genes on host cells will serve to present the peptide antigen(s) to T lymphocytes. The antigen components could also be supplied as purified MHC-peptide complexes alone or with co-stimulatory molecules that can directly signal T cells. Alternatively antibodies able to bind surface immunolgobulin and other molecules on B cells as well as antibodies able to bind the TCR and other molecules on T cells can be combined with the pharmaceutical composition of the invention.

The pharmaceutical composition of the invention may be in the form of a liposome in which protein of the present invention is combined, in addition to other pharmaceutically acceptable carriers, with amphipathic agents such as lipids which exist in aggregated form as micelies, insoluble monolayers, liquid crystals, or lamellar layers in aqueous solution. Suitable lipids for liposomal formulation include, without limitation, monoglycerides, diglycerides, sulfatides, lysolecithin, phospholipids, saponin, bile acids, and the like. Preparation of such liposomal formulations is within the level of skill in the art, as disclosed, for example, in U.S. Pat. No. 4,235,871; U.S. Pat. No. 4,501,728; U.S. Pat. No. 4,837,028; and U.S. Pat. No. 4,737,323, all of which are incorporated herein by reference.

As used herein, the term “therapeutically effective amount” means the total amount of each active component of the pharmaceutical composition or method that is sufficient to show a meaningful patient benefit, i.e., treatment, healing, prevention or amelioration of the relevant medical condition, or an increase in rate of treatment, healing, prevention or amelioration of such conditions. When applied to an individual active ingredient, administered alone, the term refers to that ingredient alone. When applied to a combination, the term refers to combined amounts of the active ingredients that result in the therapeutic effect, whether administered in combination, serially or simultaneously.

In practicing the method of treatment or use of the present invention, a therapeutically effective amount of protein of the present invention is administered to a mammal having a condition to be treated. Protein of the present invention may be administered in accordance with the method of the invention either alone or in combination with other therapies such as treatments employing cytokines, lymphokines or other hematopoietic factors. When co-administered with one or more cytokines, lymphokines or other hematopoietic factors, protein of the present invention may be administered either simultaneously with the cytokine(s), lymphokine(s), other hematopoietic factor(s), thrombolytic or anti-thrombotic factors, or sequentially. If administered sequentially, the attending physician will decide on the appropriate sequence of administering protein of the present invention in combination with cytokine(s), lymphokine(s), other hematopoietic factor(s), thrombolytic or anti-thrombotic factors.

Administration of protein of the present invention used in the pharmaceutical composition or to practice the method of the present invention can be carried out in a variety of conventional ways, such as oral ingestion, inhalation, topical application or cutaneous, subcutaneous, intraperitoneal, parenteral or intravenous injection. Intravenous administration to the patient is preferred.

When a therapeutically effective amount of protein of the present invention is administered orally, protein of the present invention will be in the form of a tablet, capsule, powder, solution or elixir. When administered in tablet form, the pharmaceutical composition of the invention may additionally contain a solid carrier such as a gelatin or an adjuvant. The tablet, capsule, and powder contain from about 5 to 95% protein of the present invention, and preferably from about 25 to 90% protein of the present invention. When administered in liquid form, a liquid carrier such as water, petroleum, oils of animal or plant origin such as peanut oil, mineral oil, soybean oil, or sesame oil, or synthetic oils may be added. The liquid form of the pharmaceutical composition may further contain physiological saline solution, dextrose or other saccharide solution, or glycols such as ethylene glycol, propylene glycol or polyethylene glycol. When administered in liquid form, the pharmaceutical composition contains from about 0.5 to 90% by weight of protein of the present invention, and preferably from about 1 to 50% protein of the present invention.

When a therapeutically effective amount of protein of the present invention is administered by intravenous, cutaneous or subcutaneous injection, protein of the present invention will be in the form of a pyrogen-free, parenterally acceptable aqueous solution. The preparation of such parenterally acceptable protein solutions, having due regard to pH, isotonicity, stability, and the like, is within the skill in the art. A preferred pharmaceutical composition for intravenous, cutaneous, or subcutaneous injection should contain, in addition to protein of the present invention, an isotonic vehicle such as Sodium Chloride Injection, Ringer's Injection, Dextrose Injection, Dextrose and Sodium Chloride Injection, Lactated Ringer's Injection, or other vehicle as known in the art. The pharmaceutical composition of the present invention may also contain stabilizers, preservatives, buffers, antioxidants, or other additives known to those of skill in the art.

The amount of protein of the present invention in the pharmaceutical composition of the present invention will depend upon the nature and severity of the condition being treated, and on the nature of prior treatments which the patient has undergone. Ultimately, the attending physician will decide the amount of protein of the present invention with which to treat each individual patient. Initially, the attending physician will administer low doses of protein of the present invention and observe the patient's response. Larger doses of protein of the present invention may be administered until the optimal therapeutic effect is obtained for the patient, and at that point the dosage is not increased further. It is contemplated that the various pharmaceutical compositions;used to practice the method of the present invention should contain about 0.01 μg to about 100 mg (preferably about 0.1 ng to about 10 mg, more preferably about 0.1 μg to about 1 mg) of protein of the present invention per kg body weight.

The duration of intravenous therapy using the pharmaceutical composition of the present invention will vary, depending on the severity of the disease being treated and the condition and potential idiosyncratic response of each individual patient. It is contemplated that the duration of each application of the protein of the present invention will be in the range of 12 to 24 hours of continuous intravenous administration. Ultimately the attending physician will decide on the appropriate duration of intravenous therapy using the pharmaceutical composition of the present invention.

Protein of the invention may also be used to immunize animals to obtain polyclonal and monoclonal antibodies which specifically react with the protein. As used herein, the term “antibody” includes without limitation a polyclonal antibody, a monoclonal antibody, a chimeric antibody, a single-chain antibody, a CDR-grafted antibody, a humanized antibody, or fragments thereof which bind to the indicated protein. Such term also includes any other species derived from an antibody or antibody sequence which is capable of binding the indicated protein.

Antibodies to a particular protein can be produced by methods well known to those skilled in the art. For example, monoclonal antibodies can be produced by generation of antibody-producing hybridomas in accordance with known methods (see for example, Goding, 1983, Monoclonal antibodies: principles and practice, Academic Press Inc., New York; and Yokoyama, 1992, “Production of Monoclonal Antibodies” in Current Protocols in Immunology, Unit 2.5, Greene Publishing Assoc. and John Wiley & Sons). Polyclonal sera and antibodies can be produced by inoculation of a mammalian subject with the relevant protein or fragments thereof in accordance with known methods. Fragments of antibodies, receptors, or other reactive peptides can be produced from the corresponding antibodies by cleavage of and collection of the desired fragments in accordance with known methods (see for example, Goding, supra; and Andrew et al., 1992, “Fragmentation of Immunoglobulins” in Current Protocols in Immunology, Unit 2.8, Greene Publishing Assoc. and John Wiley & Sons). Chimeric antibodies and single chain antibodies can also be produced in accordance with known recombinant methods (see for example, U.S. Pat. Nos. 5,169,939, 5,194,594, and 5,576,184). Humanized antibodies can also be made from corresponding murine antibodies in accordance with well known methods (see for example, U.S. Pat. Nos. 5,530,101, 5,585,089, and 5,693,762). Additionally, human antibodies may be produced in non-human animals such as mice that have been genetically altered to express human antibody molecules (see for example Fishwild et al., 1996, Nature Biotechnology 14: 845-851; Mendez et al., 1997, Nature Genetics 15: 146-156 (erratum Nature Genetics 16: 410); and U.S. Pat. Nos. 5,877,397 and 5,625,126). Such antibodies may be obtained using either the entire protein or fragments thereof as an immunogen. The peptide immunogens additionally may contain a cysteine residue at the carboxyl terminus, and are conjugated to a hapten such as keyhole limpet hemocyanin (KLH). Methods for synthesizing such peptides are known in the art, for example, as in R. P. Merrifield, J. Amer. Chem. Soc. 85, 2149-2154 (1963); J. L. Krstenansky, et al., FEBS Lett. 211, 10 (1987).

Monoclonal antibodies binding to the protein of the invention may be useful diagnostic agents for the immunodetection of the protein. Neutralizing monoclonal antibodies binding to the protein may also be useful therapeutics for both conditions associated with the protein and also in the treatment of some forms of cancer where abnormal expression of the protein is involved. In the case of cancerous cells or leukemic cells, neutralizing monoclonal antibodies against the protein may be useful in detecting and preventing the metastatic spread of the cancerous cells, which may be mediated by the protein.

For compositions of the present invention which are useful for bone, cartilage, tendon or ligament regeneration, the therapeutic method includes administering the composition topically, systematically, or locally as an implant or device. When administered, the therapeutic composition for use in this invention is, of course, in a pyrogen-free, physiologically acceptable form. Further, the composition may desirably be encapsulated or injected in a viscous form for delivery to the site of bone, cartilage or tissue damage. Topical administration may be suitable for wound healing and tissue repair. Therapeutically useful agents other than a protein of the invention which may also optionally be included in the composition as described above, may alternatively or additionally, be administered simultaneously or sequentially with the composition in the methods of the invention. Preferably for bone and/or cartilage formation, the composition would include a matrix capable of delivering the protein-containing composition to the site of bone and/or cartilage damage, providing a structure for the developing bone and cartilage and optimally capable of being resorbed into the body. Such matrices may be formed of materials presently in use for other implanted medical applications.

The choice of matrix material is based on biocompatibility, biodegradability, mechanical properties, cosmetic appearance and interface properties. The particular application of the compositions will define the appropriate formulation. Potential matrices for the compositions may be biodegradable and chemically defined calcium sulfate, tricalciumphosphate, hydroxyapatite, polylactic acid, polyglycolic acid and polyanhydrides. Other potential materials are biodegradable and biologically well-defined, such as bone or dermal collagen. Further matrices are comprised of pure proteins or extracellular matrix components. Other potential matrices are nonbiodegradable and chemically defined, such as sintered hydroxapatite, bioglass, aluminates, or other ceramics. Matrices may be comprised of combinations of any of the above mentioned types of material, such as polylactic acid and hydroxyapatite or collagen and tricalciumphosphate. The bioceramics may be altered in composition, such as in calcium-luminate-phosphate and processing to alter pore size, particle size, particle shape, and biodegradability.

Presently preferred is a 50:50 (mole weight) copolymer of lactic acid and glycolic acid in the form of porous particles having diameters ranging from 150 to 800 microns. In some applications, it will be useful to utilize a sequestering agent, such as carboxymethyl cellulose or autologous blood clot, to prevent the protein compositions from disassociating from the matrix.

A preferred family of sequestering agents is cellulosic materials such as alkylcelluloses (including hydroxyalkylcelluloses), including methylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, and carboxymethylcellulose, the most preferred being cationic salts of carboxymethylcellulose (CMC). Other preferred sequestering agents include hyaluronic acid, sodium alginate, poly(ethylene glycol), polyoxyethylene oxide, carboxyvinyl polymer and poly(vinyl alcohol). The amount of sequestering agent useful herein is 0.5-20 wt %, preferably 1-10 wt % based on total formulation weight, which represents the amount necessary to prevent desorbtion of the protein from the polymer matrix and to provide appropriate handling of the composition, yet not so much that the progenitor cells are prevented from infiltrating the matrix, thereby providing the protein the opportunity to assist the osteogenic activity of the progenitor cells.

In further compositions, proteins of the invention may be combined with other agents beneficial to the treatment of the bone and/or cartilage defect, wound, or tissue in question. These agents include various growth factors such as epidermal growth factor (EGF), platelet derived growth factor (PDGF), transforming growth factors (TGF-α and TGF-β), and insulin-like growth factor (IGF).

The therapeutic compositions are also presently valuable for veterinary applications. Particularly domestic animals and thoroughbred horses, in addition to humans, are desired patients for such treatment with proteins of the present invention.

The dosage regimen of a protein-containing pharmaceutical composition to be used in tissue regeneration will be determined by the attending physician considering various factors which modify the action of the proteins, e.g., amount of tissue weight desired to be formed, the site of damage, the condition of the damaged tissue, the size of a wound, type of damaged tissue (e.g., bone), the patient's age, sex, and diet, the severity of any infection, time of administration and other clinical factors. The dosage may vary with the type of matrix used in the reconstitution and with inclusion of other proteins in the pharmaceutical composition. For example, the addition of other known growth factors, such as IGF I (insulin like growth factor I), to the final composition, may also effect the dosage. Progress can be monitored by periodic assessment of tissue/bone growth and/or repair, for example, X-rays, histomorphometric determinations and tetracycline labeling.

Polynucleotides of the present invention can also be used for gene therapy. Such polynucleotides can be introduced either in vivo or ex vivo into cells for expression in a mammalian subject. Polynucleotides of the invention may also be administered by other known methods for introduction of nucleic acid into a cell or organism (including, without limitation, in the form of viral vectors or naked DNA).

Cells may also be cultured ex vivo in the presence of proteins of the present invention in order to proliferate or to produce a desired effect on or activity in such cells. Treated cells can then be introduced in vivo for therapeutic purposes.

Patent and literature references cited herein are incorporated by reference as if fully set forth.

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ataactggag taaaacccac ttagatttct atgtccccaa acctctggtg tggtcagggt 720 tggcacctgc cctctcaacc atttgtctca ctgtacatgc atcttgtcta tgtcttccac 780 tagagaccat gagggcagag atcagaccta tgtacgttgc acattgctgt ccccagtacc 840 tagcacagca ccttgcccca gtacgcactt catatatatt tcctggacta cggcaggtga 900 gccctttgtg agggttccac ctgcccactg gcctggcctt taatgtcagg ggagcatttc 960 tgatatatta atgcccctct aattgtgctg cattcgttta cataggcagt gcagcagcct 1020 ggctttggtg tttaaagacc ggattgcagt caaagctctg ctgtttgctg gctatgaact 1080 ccaggtaagt tgccaggttc ctctgagcac taatgataat attacctgcc tcacagggtt 1140 gttttgagag cagcttctgc tgctgcccca tgccccagaa ttatggaaaa ccattttgta 1200 aacttcaagt cacttcctct ccatagtaca gatcaatggt agaccagtga tcagggagga 1260 tacaaatcat aaccccaaaa aaggcttctt tgttgtattt tacctcaagt gttttcttag 1320 agaacctcaa caaaccacac tattttctag taatcagcca cttatcccac catttgcagt 1380 aaggaaaact gaggcacgcc ttgatggctt attcagcatc agcagcctca caaaagacag 1440 aagtctcctt tggattagct ttatcatctt tcccttaagc agagatgatg gtgcctttct 1500 cgctgctctg gctcagttaa gaagtcaagt ctgatttatt ggtcatccta actatcgttt 1560 cctgaaggcc cgaagccctg taatgctgtt gtctggcttc ccagatttat gaccatggtt 1620 tctggccccc aacaatatct ggagttcggt ttacatattc acttccacca tccaatccaa 1680 atcctcccag gcagcaatca agctggggct gattcctcat ccatttgtgg gctcactttt 1740 tctggcaagt cagccttcat tctccaggac gcttagaagc cgcatgttgg cggtggattg 1800 tgctacggga aagagtgaat gtgtagcctg cacatttgaa gccttgctgg ggtagagagc 1860 aacgctactg ctcctggaat gtccaggcca ctgttagaaa ggccatctta ttccttagaa 1920 gagtctagcc ctgctgcagg cttcagaaac gtgtgctcta agctcgttcc tgctcatttg 1980 aagcagtctt ctgaaaaggt ctgcagaaac ctgcctttac cctctccctc atcctgcgtg 2040 gcctttgtca catccttcct ccaaggttcc tctggtggtg gtagtaggga ggctgccacc 2100 tggctttgca tgtgggaaag cccagcctct tccctccacc ctcacagcag gacagccaaa 2160 cttggatttt ttcatgagga agcaactctt atgagctctc tggttcagct ctctggttaa 2220 aagaccatac tgtgctgttt ctggggcagc acagacctgg ttgatcgtgt ccacaggaag 2280 aacagccttt gggattcatt agtctggtta agaccagccc tgcagcctcc tctgccagct 2340 atagaactat gtgttagagt tggtgctgaa gccagtcgca aacccatccc agatgcgtct 2400 ggtcttgttg atgttcaaat gccacctcct cctccaggaa gacttcacca cctccccaag 2460 gctgccttat gggctccttc tctgttccct ctcgactctc cccctctatc actatggcca 2520 ttttatagaa ttttaattat tgtctcgggt gtctccacta gactgtaagt atcaagtgtg 2580 tagagacttt tgtttcaact ctgtatcccc aaaattcagc atagttcata gcacatacag 2640 tactctcaat gcctgttgaa tgaataaaga gtctgcttgc atgtaaaact acagtggttt 2700 ggtcttggag acacttgttt tggaattctt ctactgatat ggacagcatc aagatgatgg 2760 gaaatgtatt ggtctgggat ttgttttgcc tacaaagttt cttatgttgg ctcatctcca 2820 actagataaa accctgagtc taggcttccc cttctaacaa agctgctata cctttatgga 2880 cctccatttt cctgtctgta aaatgagagt gtgggctagc tagaaaaatt tctggtgtcc 2940 cccttgctgc tttgtaattc tggagtacgt tcggagaaca ccccaatgtg acaaaggatc 3000 tggaaattct tcataaaata ttcagggagg gagacaactc agggaacatg acaactgtct 3060 ggaattattt gaggggttgt catgtagaag atgaaaagga ttagattatc ttgaaaggcc 3120 ccacaggtta taaataagac caattattaa ttcattcaac aaatatttga gtacctgcca 3180 tgtgcaaggc actattctaa gcaataatga tgcagtaatg aatacaacag acaaaaatct 3240 tgttgccttt atggagttga cattctagtg aacagaaaca attcaaaaac aaacacaatg 3300 gagaggagct tcttggaccc tcaaaacgag ctgcctgtga actattgagc tctttgtgtt 3360 caggaatacg tttagtactt agaaatctgc ttccagtggc tgcttagact aaatgacctt 3420 gttaggtttt tttagcccag caatcccatg aatctaaggc tagcgaagat gtgtgatctc 3480 tctattctaa caccactaag ccaaatcatg acctcctctc aatggtaact gtcactctaa 3540 aaagagagat aaggtagatg cagtgggctg ttcttatgaa aaggcaccta aaaaatagta 3600 ctttagaaac atgcattgtg gtgggggtct gggtggaggg gttgcttttt cttgagatcc 3660 ctgtgatatt gaggatgaag aaagagaaac acagggggtg ggcaacttcc ttgaaggacc 3720 agagagagtg agtcatgagg aagagaagga ggagacagag aacaggagag ttggggatga 3780 agcctttgat gaggggagtg aggaggggca gaagtaggag acagacatga ggaaaccacc 3840 aactgaagtc ccagaaaccc agcctccgtc ccctctaggt cctactgccg tcatcctctt 3900 tctgtaaagg tgagagtcta ggtgcagtgt cccaggttcc aaacacaagt tcatactcat 3960 tgactagtgg gatgcccact gtgagagcag gaaggagggc tagagagatc taagagggca 4020 gaagccctgc cctgccagta ttttttgcct ccagccacct gctctgttct gagacatgcc 4080 tgagaccagc tgcctacagg gggaccaggg tctgtttctg ctgttaacct tggttccctc 4140 ctgcattcct gcatgtgggg atgtagacag gaagcctgca ggtatggagc aattgaagca 4200 gagtctagat agagcccaga ctccttactt cccatagtac tattctgcat tttgtagtgc 4260 tgcttatgct tttcagtgtt tccacatcta tttactaata acatcatagt acaacagcaa 4320 gaacatggcc tcagaactca aagttctgga attctaatat tttatttgat tgtcagtatt 4380 tctgtgagat agataaaata ggaattattt cctctgatct gcaggtgagg aaactcagtc 4440 acagggagca catttatcca tacttgtgga gctatagtat aactagtatt aggacaagga 4500 tagccaacat agttaaaaaa aaaaaaaaa 4529 <210> SEQ ID NO 6 <211> LENGTH: 98 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 6 Met Ile Ser Met Ile Lys Met Phe Arg Glu Arg Asn Ile Leu Arg Asp 1 5 10 15 Asn Trp Ser Lys Thr His Leu Asp Phe Tyr Val Pro Lys Pro Leu Val 20 25 30 Trp Ser Gly Leu Ala Pro Ala Leu Ser Thr Ile Cys Leu Thr Val His 35 40 45 Ala Ser Cys Leu Cys Leu Pro Leu Glu Thr Met Arg Ala Glu Ile Arg 50 55 60 Pro Met Tyr Val Ala His Cys Cys Pro Gln Tyr Leu Ala Gln His Leu 65 70 75 80 Ala Pro Val Arg Thr Ser Tyr Ile Phe Pro Gly Leu Arg Gln Val Ser 85 90 95 Pro Leu <210> SEQ ID NO 7 <211> LENGTH: 3537 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 7 aacttagatt tcttaaaact gtatacagat aactaatttt tattttgaaa tagcttttat 60 gttcttgtgt ttatgtaata gtcacattaa ttttgctctt ttggctttgt gttgtgttta 120 tttgatgact gttttattcg gtttaatttt ttcttgattt tgcaaattca tttttatcat 180 ctttaagtgg tggagtggcc atttcagctt gaaatatttc actgtcttta taatttcatt 240 ccatgcatgt gttttgtgtt tgtgacggtg tggtggtatt tagtctatag aagaacatgt 300 ggagcaggtc aaccaaaact gcatagcaga agattgccac atcaaggtag tattccaaga 360 tcttgtattt agctcattct ttaaagttca aggagctaac gcctcatctc tgatactaac 420 catgacctgc ccaactggct aactactcag agaactcata gtactcccat accacttcag 480 tggcacaggg gaggagatgc ttcactgtat ctggcttgct ctgtcttgcc cttggttctt 540 ctctttcttg ctccctgtcc catcttcact tgtcactttt tctgttttaa gcatggctgt 600 ttcatcttct tgattctgcc ttttctttcc ttcccatcac caaccctaag ccattgcatc 660 ttcctctcat cagtctcttt tattcctttc gaagtatccc tctttccaac ttttccttat 720 ttctgtctca ccacccttac ttcaaagggt ggtttctttg cggttttcta tggcttttta 780 ctccactctg tgcctcttaa tgtatacaca ttcttattgc agaatattta tgcacttttg 840 gaagagctaa gagagacata ctactgtata aattactaat aaaaatatat tagccatgtt 900 ttataattaa tcagtatctt accatcacag tggaaattgg ggtgattaca ggacatcaga 960 gaatttaagc aaattttcca aagctagttt tcaacacatt aaagttactc ttaccctttt 1020 ttcttgctgc tgctgctgct gctacatttt cttcttatcc tacatttaaa tcttatggga 1080 tgtgcataac tctaaataga gctgtgctgc agcaactaaa actgctgatg aatgttttct 1140 aggttgaagc tgatctgggc tatccaggtg gaaaggcgaa agtcatccat aaggaatctg 1200 atatgatcat ggcattttct gttaataagg caaattgtaa tgaaattgtt ttggcttcaa 1260 cacatgatgt tcaagaactt gatgttactt ctctactggc ctgtcagtca tacatatgga 1320 tcggagaaga atatgacaga gaatccaaaa gttcagatga tgttgattat cgtggttcca 1380 ctacaactct ttatcaaccc agtgcaacat cctattcagc aagtcaggtg catccacctt 1440 catctctgcc atggctgggc actggacaga ctagcactgg agctagtgtg cttatgaaaa 1500 ggaatctaca taatgttaag agaatgactt cacacccagt ccatcaatac tatcttacag 1560 gtgctcagga cggcagtgta cgaatgtttg aatggacgcg gcctcagcaa cttgtctgct 1620 ttcgtcaagc tggcaatgca agagttacta gattatattt taattcacaa ggcaacaagt 1680 gtggtgttgc ggatggagag ggttttctga gtatctggca agttaaccaa actgcatcaa 1740 atcctaaacc ttatatgagt tggcagtgcc acagtaaagc cacaagtgac tttgcattta 1800 ttacctcttc aagtctagtt gccacatctg gacactccaa tgacaataga aatgtttgcc 1860 tctgggacac attaatatca cccggaaaca gcctcattca tggtttcacg tgccacgatc 1920 atggtgccac ggtactgcag tatgcaccca aacagcaact cctaatctcg gggggtagga 1980 aaggacacgt ctgcattttt gacatcaggc aaaggcagct cattcacacg ttccaggccc 2040 atgactcagc tattaaggct ctggccttgg atccctatga ggaatatttt accacaggtt 2100 cagcagaagg taacataaag gtttggagat tgacaggcca tggcctaatt cattcattta 2160 aaagtgaaca tgctaagcag tccatatttc gaaacattgg ggctggagtc atgcagattg 2220 acatcatcca gggcaatcgg ctcttctcct gtggtgcaga tggcacgctg aaaaccaggg 2280 ttttgcccaa tgcttttaac atccctaaca gaattcttga cattctataa agattggggt 2340 tttattttta tatacatttc agttaaaagg cacactacag tcatcactag gcaattctgc 2400 tttctaagca gttgtattga aaacagagaa tctctgtgta gaatttgaat atgacccaag 2460 ctgagtatta tctaaacagg ttggtggaat gaatgcgcat gtaccttatt atgctgacat 2520 actaaaaaaa ataaaaccta gtattgtatg aaggatagct attctttaca gcatttagca 2580 aacctgattc agaaaacatt tgagattagc aaattagtaa cttgaaataa tgaaaaggac 2640 gtttatacca aattaaggaa gaaaatgttg ctgatttggg tttttcttcc tgttcttacc 2700 actgactgaa gcatgcctgc agtctcctcc tctgttgaat gaaggataat cataaggtgt 2760 ttgttaggag cgctagacca cctggaaaac tttcttagct gtggagcagt gcgcagtgac 2820 cagttctctg ctgtgagagg ccgtttccat tctttcctgc tgaatatttt tcctgttagt 2880 gtttatactg agctagtact gtaacttgca aatgagtgca aatttaaatg caatgtttta 2940 ctcacaattt gcacattcac attttttgga ctgctagttt ttctatttaa atatttgcct 3000 tcatgttagg aatgtactat gtgaacatga catatttgta gttaaccaaa cacaccttct 3060 tagtccagtt tagtactttt tcttttcgtg tattcaaggt taaacaccca aacatttaag 3120 gatatgttga aactacacca atagagcatt tcatatcata attaaaatga atgttaggct 3180 tcttgtggcc agttaatagt tgatgagatt ggtgacatta tttattgcca cagcctattg 3240 tataaactat gcagagttaa atatttgctt gtaaaatatt agccaatgtt gtcattattt 3300 tgatgtattt ccttggttat gaccaaaaat atgttgagat actgaaacta atgtctgtgt 3360 gtttaaatgt ttaccagcaa attgtcttat catgttaatg agaatgttca atgcctgtgt 3420 ggtaaatagt aaatacaatg gcataaaagt aactttctct gaagatgtga tgttcaggct 3480 gtgaaatata tatgtaaaag aaaaataaat gttatttgtt agaaaaaaaa aaaaaaa 3537 <210> SEQ ID NO 8 <211> LENGTH: 375 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 8 Met Ile Met Ala Phe Ser Val Asn Lys Ala Asn Cys Asn Glu Ile Val 1 5 10 15 Leu Ala Ser Thr His Asp Val Gln Glu Leu Asp Val Thr Ser Leu Leu 20 25 30 Ala Cys Gln Ser Tyr Ile Trp Ile Gly Glu Glu Tyr Asp Arg Glu Ser 35 40 45 Lys Ser Ser Asp Asp Val Asp Tyr Arg Gly Ser Thr Thr Thr Leu Tyr 50 55 60 Gln Pro Ser Ala Thr Ser Tyr Ser Ala Ser Gln Val His Pro Pro Ser 65 70 75 80 Ser Leu Pro Trp Leu Gly Thr Gly Gln Thr Ser Thr Gly Ala Ser Val 85 90 95 Leu Met Lys Arg Asn Leu His Asn Val Lys Arg Met Thr Ser His Pro 100 105 110 Val His Gln Tyr Tyr Leu Thr Gly Ala Gln Asp Gly Ser Val Arg Met 115 120 125 Phe Glu Trp Thr Arg Pro Gln Gln Leu Val Cys Phe Arg Gln Ala Gly 130 135 140 Asn Ala Arg Val Thr Arg Leu Tyr Phe Asn Ser Gln Gly Asn Lys Cys 145 150 155 160 Gly Val Ala Asp Gly Glu Gly Phe Leu Ser Ile Trp Gln Val Asn Gln 165 170 175 Thr Ala Ser Asn Pro Lys Pro Tyr Met Ser Trp Gln Cys His Ser Lys 180 185 190 Ala Thr Ser Asp Phe Ala Phe Ile Thr Ser Ser Ser Leu Val Ala Thr 195 200 205 Ser Gly His Ser Asn Asp Asn Arg Asn Val Cys Leu Trp Asp Thr Leu 210 215 220 Ile Ser Pro Gly Asn Ser Leu Ile His Gly Phe Thr Cys His Asp His 225 230 235 240 Gly Ala Thr Val Leu Gln Tyr Ala Pro Lys Gln Gln Leu Leu Ile Ser 245 250 255 Gly Gly Arg Lys Gly His Val Cys Ile Phe Asp Ile Arg Gln Arg Gln 260 265 270 Leu Ile His Thr Phe Gln Ala His Asp Ser Ala Ile Lys Ala Leu Ala 275 280 285 Leu Asp Pro Tyr Glu Glu Tyr Phe Thr Thr Gly Ser Ala Glu Gly Asn 290 295 300 Ile Lys Val Trp Arg Leu Thr Gly His Gly Leu Ile His Ser Phe Lys 305 310 315 320 Ser Glu His Ala Lys Gln Ser Ile Phe Arg Asn Ile Gly Ala Gly Val 325 330 335 Met Gln Ile Asp Ile Ile Gln Gly Asn Arg Leu Phe Ser Cys Gly Ala 340 345 350 Asp Gly Thr Leu Lys Thr Arg Val Leu Pro Asn Ala Phe Asn Ile Pro 355 360 365 Asn Arg Ile Leu Asp Ile Leu 370 375 <210> SEQ ID NO 9 <211> LENGTH: 1466 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 9 ccgcgcagga ggacggagcc ctaaccgcaa cccgcgccgc gccgcgccga tttgatttgt 60 atccactgtc accagcactg ctcacttagg actttctgga tccggaccca ggcagcgcac 120 actggactct tgaggaagaa ggagactcta attttggatt ccttggtgga ggaaaataaa 180 acactctggt cttgccgcca acgatgcaag tgtgactgct ggcgtcttca tgagctccag 240 aggtcacagc acgctaccaa ggactctcat ggcccctcgg atgatttccg agggagacat 300 argaggcatt gctcaaatca cctcctctct attcctgggc agaggcagtg tggcctccaa 360 tcggcacctc ctccaggctc gtggcatcac ctgcattgtt aatgctacca ttgagatccc 420 taatttcaac tggccccaat ttgagtatgt taaagtgcct ctggctgaca tgccgcatgc 480 ccccattgga ctgtactttg acaccgtggc tgacaagatc cacagtgtga gcaggaagca 540 cggggccacc ttggtgcact gtgctgcagg ggtgagccgc tcagccacgc tgtgtatcgc 600 gtacctgatg aaattccaca acgtgtgcct gctggaggcg tacaactggg tgaaagcccg 660 gcgacctgtc atcaggccca acgtaggctt ctggaggcaa ctgatagact acgagcgcca 720 gctctttggg aagtcgacag ttaaaatggt acagacacct tatggcatag ttcccgacgt 780 ctatgagaag gagtcccgac acctgatgcc ttactggggg atttagtgcc actgaagcct 840 gcgtcagcag cccgagcggg gccggcatct gctccccgcc gtctgctccc tctccactct 900 cttctcaaat ggctgacttc tggttctccc tcaagtgttt tttacactgg gtgttcaaat 960 ttattttaag agatagggag ggaggggaca taaagggaat gcatacattg ctagtcacat 1020 ttttaaaatt aacattttgg aatagtgttt atggaaatct ttagctttta atcattttta 1080 ccaatttgaa cagtttaata aactggttct gctctcttct gaatctcakg ccttkggcac 1140 cttggtaggt gcaggaggag ctcagtgcaa aaatcacttt ggggcctcat taacccttta 1200 gagacaagyt ttgccccagg ytgcggacca gacagatgyt tagggaaggt tgataccagc 1260 ttcagtctct astggattag ccctactctt tcctttcccc tccattattt agtgactctg 1320 taagtaagtt aaatacaccc ttattattta gctgttaagt aactataatg aaatctgctg 1380 caaaatctct cttggaatcc atgtgcccag gattatatta gcattatttt taataaatct 1440 atatgcttaa caaaaaaaaa aaaaaa 1466 <210> SEQ ID NO 10 <211> LENGTH: 198 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (25) <400> SEQUENCE: 10 Met Ser Ser Arg Gly His Ser Thr Leu Pro Arg Thr Leu Met Ala Pro 1 5 10 15 Arg Met Ile Ser Glu Gly Asp Ile Xaa Gly Ile Ala Gln Ile Thr Ser 20 25 30 Ser Leu Phe Leu Gly Arg Gly Ser Val Ala Ser Asn Arg His Leu Leu 35 40 45 Gln Ala Arg Gly Ile Thr Cys Ile Val Asn Ala Thr Ile Glu Ile Pro 50 55 60 Asn Phe Asn Trp Pro Gln Phe Glu Tyr Val Lys Val Pro Leu Ala Asp 65 70 75 80 Met Pro His Ala Pro Ile Gly Leu Tyr Phe Asp Thr Val Ala Asp Lys 85 90 95 Ile His Ser Val Ser Arg Lys His Gly Ala Thr Leu Val His Cys Ala 100 105 110 Ala Gly Val Ser Arg Ser Ala Thr Leu Cys Ile Ala Tyr Leu Met Lys 115 120 125 Phe His Asn Val Cys Leu Leu Glu Ala Tyr Asn Trp Val Lys Ala Arg 130 135 140 Arg Pro Val Ile Arg Pro Asn Val Gly Phe Trp Arg Gln Leu Ile Asp 145 150 155 160 Tyr Glu Arg Gln Leu Phe Gly Lys Ser Thr Val Lys Met Val Gln Thr 165 170 175 Pro Tyr Gly Ile Val Pro Asp Val Tyr Glu Lys Glu Ser Arg His Leu 180 185 190 Met Pro Tyr Trp Gly Ile 195 <210> SEQ ID NO 11 <211> LENGTH: 1521 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 11 aatttcttgg gcatttaccc atgccagaag gctaacctgg ggggaggggg gcgcttgtgc 60 tggtgaggca cttggataca tactgatgct gcaagttcag gggatttttc ttactcttag 120 gtttaaccaa gaacactgag cagggaaaaa ccctgccttt cctaactgca tgtatttttt 180 cctttttgga aaggtggtag agactcagaa gctttccttg ttttcttcag gcctgctccc 240 agttttctta acagtttctt ttgttgcttt ctctctccct tgttgctttc catggcagta 300 atcctcctag agtccaagca gtctgttgta tggagcaggg tgtgtgggtt ttctgggccc 360 atcattatgg ctgcttcaga gtcagaagaa agccataggg cagtagggga gctcctattg 420 cctarcccct ctccctttgt ggctcccact ctagctgcct atttttgctc atcagctggt 480 gagtcagtat gggccagcag ttctccctcc ctaagccctt gctactttat gggttagctt 540 tgcaggtttg gtggcttgag gggtgggggc aactcaccac tgccaggtaa ctccctgaag 600 ggtgggagtg gattatcttc taggctctta cccgcggtag ggaagggcat caacactgtc 660 ttccttccat tctcctttcc cccatcccat ttagtgctgc cacagggcag aagcacacaa 720 accaaccaca cagtctctga cttctcctaa gcactttgag ttgttgaatg gggctcaggg 780 gcaagagttt ttgctgccct ccccagcgtg gtcacagggt tattgaactg cctgcacttg 840 tttctcatgc aactccagca ttttccccag aagttgaact atggatagca gcttggtatg 900 gatttcctaa atcttaacat ttgaagcagc ttcttgaggc tggcaactat cctggtttct 960 gtcttggagg gggtggtttg tttgctgggg cccaacgtct gtcccaagtg gtggggtgag 1020 agtaagttaa ctttggtgcc aggtgagagg tgggggctct ttgcttagac tccctatcat 1080 ggaaagattg gagttttcta tgcagggcac tggggaaaag gattgctgat tctgactgac 1140 cctgatcaga gagattagga ttgtattttg acataggatt tggaacccat ctaaatgttg 1200 aagttccctg agacrgctct ccagctgctg agcctgcgcc aggggytaag cagcccctaa 1260 tgagaggctc tgctcccttt cccacctcgc caatgttgtt gttgctgcct ttttgatttg 1320 tatcctctgt tatagacatt ttttraaaac gatttcctct ttcattgtgc acaagtgctg 1380 agagtctgag gccccatttc tgctgtgtat atatatcctg actcggggct tttattcagc 1440 aaactgttca ttcttctgtc agacaatgtc atattcaact ctgttcatat taaaccactg 1500 tgaagcaaaa aaaaaaaaaa a 1521 <210> SEQ ID NO 12 <211> LENGTH: 81 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (45) <400> SEQUENCE: 12 Met Ala Val Ile Leu Leu Glu Ser Lys Gln Ser Val Val Trp Ser Arg 1 5 10 15 Val Cys Gly Phe Ser Gly Pro Ile Ile Met Ala Ala Ser Glu Ser Glu 20 25 30 Glu Ser His Arg Ala Val Gly Glu Leu Leu Leu Pro Xaa Pro Ser Pro 35 40 45 Phe Val Ala Pro Thr Leu Ala Ala Tyr Phe Cys Ser Ser Ala Gly Glu 50 55 60 Ser Val Trp Ala Ser Ser Ser Pro Ser Leu Ser Pro Cys Tyr Phe Met 65 70 75 80 Gly <210> SEQ ID NO 13 <211> LENGTH: 697 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 13 tgaagcttct gcacatgtag ttcctagagc tgctgcttat taaaatgtca acatcttcat 60 cttctagctg ggacaacctc ttagagtctc tctctctcag cacagtatgg aattggatac 120 aagcaagttt tttgggagag actagtgcac ctcagcaaac aagtttggga ctattatata 180 atcttgctcc agctgtgcaa atcatcttga ggatttcttt cttgatttta ttgggaatag 240 gaatatatgc cttatggaaa cgaagtattc agtcaattca gaaaacattg ttgtttgtaa 300 tcacactcta caaactttac aagaagggct cacatatttt tgaggctttg ctagccaacc 360 cagaaggaag tggtctccga attcaagaca ataataatct tttcctgtcc ttgggtctgc 420 aagagaaaat tttgaaaaaa cttaagacag tggaaaacaa aatgaagaac ctagaaggga 480 taatcgttgc tcaaaaacct gccacgaaga gggattgctc ctctgagccc tactgcagct 540 gctctgactg ccagagtccc ttgtccacat cagggtttac ttcccccatt tgaaatgtga 600 tggactccaa tcttttccag gaaagcactg tttccctcat gtgtgcagtg gtgtatcaat 660 aaagatagag aacgctattg aaaaaaaaaa aaaaaaa 697 <210> SEQ ID NO 14 <211> LENGTH: 182 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 14 Met Ser Thr Ser Ser Ser Ser Ser Trp Asp Asn Leu Leu Glu Ser Leu 1 5 10 15 Ser Leu Ser Thr Val Trp Asn Trp Ile Gln Ala Ser Phe Leu Gly Glu 20 25 30 Thr Ser Ala Pro Gln Gln Thr Ser Leu Gly Leu Leu Tyr Asn Leu Ala 35 40 45 Pro Ala Val Gln Ile Ile Leu Arg Ile Ser Phe Leu Ile Leu Leu Gly 50 55 60 Ile Gly Ile Tyr Ala Leu Trp Lys Arg Ser Ile Gln Ser Ile Gln Lys 65 70 75 80 Thr Leu Leu Phe Val Ile Thr Leu Tyr Lys Leu Tyr Lys Lys Gly Ser 85 90 95 His Ile Phe Glu Ala Leu Leu Ala Asn Pro Glu Gly Ser Gly Leu Arg 100 105 110 Ile Gln Asp Asn Asn Asn Leu Phe Leu Ser Leu Gly Leu Gln Glu Lys 115 120 125 Ile Leu Lys Lys Leu Lys Thr Val Glu Asn Lys Met Lys Asn Leu Glu 130 135 140 Gly Ile Ile Val Ala Gln Lys Pro Ala Thr Lys Arg Asp Cys Ser Ser 145 150 155 160 Glu Pro Tyr Cys Ser Cys Ser Asp Cys Gln Ser Pro Leu Ser Thr Ser 165 170 175 Gly Phe Thr Ser Pro Ile 180 <210> SEQ ID NO 15 <211> LENGTH: 983 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 15 gggcgtggtg tcttgctgtc tcaggccctt cctctgtgca tccacgtaag tgtgggtaag 60 ccaagaatag cctgggttca aatccacctt tgccgttaat tggctgtgtg ctggtagaca 120 agttacttag cttctctgtg cccccactcc ctcatctgca cgcgagaatt gtaacagagc 180 cttcctcaga gcgatgatgg tgtttaggat gacatgcgct gcacagcaag tcctggccgt 240 ggcggctgcc attgcagccc gtggggtcac cctggaggcc gtgattgctg atgttgtgct 300 gttcttgtgc cttgctctct tcttctcggt gcccccagac tctctctgcc ttcggaggac 360 ggcgtctctc tcgcctcaca ctgtgtgcac gggcagtgcg gacgggtgct ggcttggtct 420 ttccagccct gcctcgctcg gggcctgctg catcgtagct caggcctagg acccatctct 480 gtacctgcag gtcttgggtg ctgcccggca tgagtggagg agtttatcag aacaggacct 540 tttataggag gttttaactt tagaagggaa tagaaaagtg tcatggcagc aatatttatt 600 tctagatcac cctgagtttt ttttctttgt ttkgtttwat tgtcctcttt acaccatgag 660 tttttaatga tgaatgagtg aaggagtgac agtgcgggtt gagcatccct tatccagatg 720 ctccagaatc ggaaaccctc tgacaccgat gtggcacctc aggcatagct gagctagtga 780 cacctttgct ttctcatggg tcagtgtaca caaaccttgt ttcatgcaca aaattatcaa 840 aagtaccgca caaaattacc ctcaggctgt gtgtataagg tgtatatgaa acataaatga 900 atttcctgtt cagacctggg tcctatccaa acatatctca ttacgtatat acagatgttc 960 cgaatcagaa aaaaaaaaaa aaa 983 <210> SEQ ID NO 16 <211> LENGTH: 91 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 16 Met Met Val Phe Arg Met Thr Cys Ala Ala Gln Gln Val Leu Ala Val 1 5 10 15 Ala Ala Ala Ile Ala Ala Arg Gly Val Thr Leu Glu Ala Val Ile Ala 20 25 30 Asp Val Val Leu Phe Leu Cys Leu Ala Leu Phe Phe Ser Val Pro Pro 35 40 45 Asp Ser Leu Cys Leu Arg Arg Thr Ala Ser Leu Ser Pro His Thr Val 50 55 60 Cys Thr Gly Ser Ala Asp Gly Cys Trp Leu Gly Leu Ser Ser Pro Ala 65 70 75 80 Ser Leu Gly Ala Cys Cys Ile Val Ala Gln Ala 85 90 <210> SEQ ID NO 17 <211> LENGTH: 267 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 17 ggaaaacacc ctaaatgtgc atgcatctcc aagtcctcca ggagccacgc gtgctccaca 60 ttctttcttt tcctggcaca tttttggctg ccaggatgac tgagaaaata atcaaccttc 120 ccatcagtca cctgtttctc ttcctgagca gtttccttct gccactcagt caaaaggccc 180 acaaacatgt tcaccaagtc ctaacctcta gaagggagag agacttcaga gactgatttt 240 tagctgcaac caaaaaaaaa aaaaaaa 267 <210> SEQ ID NO 18 <211> LENGTH: 73 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 18 Met Cys Met His Leu Gln Val Leu Gln Glu Pro Arg Val Leu His Ile 1 5 10 15 Leu Ser Phe Pro Gly Thr Phe Leu Ala Ala Arg Met Thr Glu Lys Ile 20 25 30 Ile Asn Leu Pro Ile Ser His Leu Phe Leu Phe Leu Ser Ser Phe Leu 35 40 45 Leu Pro Leu Ser Gln Lys Ala His Lys His Val His Gln Val Leu Thr 50 55 60 Ser Arg Arg Glu Arg Asp Phe Arg Asp 65 70 <210> SEQ ID NO 19 <211> LENGTH: 679 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 19 aaacttctgg gatcacaggc atgagccacc gtgcctggcc ctgatctggg atttaaaggg 60 gcagttgctg agcaaataga agccagggca agaaaggatt tatgtgcttg ggattcttga 120 ggggttttcc agagtcagtc cccaattctg atgtttttat acgcaacact aggggtcctt 180 ctgaagttat cccggcccct gggaaactca cgtggcatgg ggcccccttc tgccctggtc 240 tctttcatcc catctgtccc ggccccagag cctgtccagt ctggtcctct ctgtcctgct 300 tggtttgtca ccatgtgatg ttgggatggc ttgtctttgc cgcctcactt cctaagctga 360 cagacgtgtc tgctagggac caccagctcc caagccgcat gacggtgctt tccttcaagg 420 ttcagaggct tccctttcag tctggcccat ctcccacatc ctaatggctc tgctgtctca 480 ggggcagctc tcctttttaa cttattggca gagctgggat gacttatagg tccctggctc 540 agtgagtaag caagttcaga gacttggctt tggccatttt gttctcttag gctcatcctt 600 ggatgccaac agggaaataa cctgccagat ttcagtcact actttttaga agttaaaaaa 660 aaaaaaaaaa aaaaaaaaa 679 <210> SEQ ID NO 20 <211> LENGTH: 120 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 20 Met Cys Leu Gly Phe Leu Arg Gly Phe Pro Glu Ser Val Pro Asn Ser 1 5 10 15 Asp Val Phe Ile Arg Asn Thr Arg Gly Pro Ser Glu Val Ile Pro Ala 20 25 30 Pro Gly Lys Leu Thr Trp His Gly Ala Pro Phe Cys Pro Gly Leu Phe 35 40 45 His Pro Ile Cys Pro Gly Pro Arg Ala Cys Pro Val Trp Ser Ser Leu 50 55 60 Ser Cys Leu Val Cys His His Val Met Leu Gly Trp Leu Val Phe Ala 65 70 75 80 Ala Ser Leu Pro Lys Leu Thr Asp Val Ser Ala Arg Asp His Gln Leu 85 90 95 Pro Ser Arg Met Thr Val Leu Ser Phe Lys Val Gln Arg Leu Pro Phe 100 105 110 Gln Ser Gly Pro Ser Pro Thr Ser 115 120 <210> SEQ ID NO 21 <211> LENGTH: 3340 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 21 ggaggaacac ggcaacttcc ttattacagt tcctggaggg tcagatggtc caagtggagt 60 actgatctgc tctgaaaact atattactta caagaacttt ggtgaccagc cagatatccg 120 ctgtccaatt cccaggaggc ggaatgacct ggatgaccct gaaagaggaa tgatttttgt 180 ctgctctgca acccataaaa ccaaatcgat gttcttcttt ttggctcaaa ctgagcaggg 240 agatatcttt aagatcactt tggagacaga tgaagatatg gttactgaga tccggctcaa 300 atattttgat actgtacccg ttgctgctgc catgtgtgtg cttaaaacag ggttcctttt 360 tgtagcatca gaatttggaa accattactt atatcaaatt gcacatcttg gagatgatga 420 tgaagaacct gagttttcat cagccatgcc tctggaagaa ggagacacat tcttttttca 480 gccmagacca cttaaaaacc ttgtgctggt tgatgagttg gacagcctct ctcccattct 540 gttttgccag atagctgatc tggccaatga agatactcca cagttgtatg tggcctgtgg 600 taggggaccc cgatcatctc tgagagtcct aagacatgga cttgaggtgt cagaaatggc 660 tgtttctgag ctacctggta accccaacgc tgtctggaca gtgcgtcgac acattgaaga 720 tgagtttgat gcctacatca ttgtgtcttt cgtgaatgcc accctagtgt tgtccattgg 780 agaaactgta gaagaagtga ctgactctgg gttcctgggg accaccccga ccttgtcctg 840 ctccttatta ggagatgatg ccttggtgca ggtctatcca gatggcattc ggcacatacg 900 agcagacaag agagtcaatg agtggaagac ccctggaaag aaaacaattg tgaagtgtgc 960 agtgaaccag cgacaagtgg tgattgccct gacaggagga gagctggtct atttcgagat 1020 ggatccttca ggacagctga atgagtacac agaacggaag gagatgtcag cagatgtggt 1080 gtgcatgagt ctggccaatg taccccctgg agagcagcgg tctcgcttcc tggctgtggg 1140 gcttgtggac aacactgtca gaatcatctc cctggatccc tcagactgtt tgcaacctct 1200 aagcatgcag gctctcccag cccagcctga gtccttgtgt atcgtggaaa tgggtgggac 1260 tgagaagcag gatgagctgg gtgagagggg ctcgattggc ttcctatacc tgaatattgg 1320 gctacagaac ggtgtgctgc tgaggactgt cttggaccct gtcactgggg atttgtctga 1380 tactcgcact cggtacctgg ggtcccgtcc tgtgaagctc ttccgagtcc gaatgcaagg 1440 ccaggaggca gtattggcca tgtcaagccg ctcatggttg agctattctt accaatctcg 1500 cttccatctc accccactgt cttacgagac actggaattt gcatcgggtt ttgcctcgga 1560 acagtgtccc gagggcattg tggccatctc caccaacacc ctacggattt tggcattaga 1620 gaagctcggt gctgtcttca atcaagtagc cttcccactg cagtacacac ccaggaaatt 1680 tgtcatccac cctgagagta acaaccttat tatcattgaa acggaccaca atgcctacac 1740 tgaggccacg aaagctcaga gaaagcagca gatggcagag gaaatggtgg aagcagcagg 1800 ggaggatgag cgggagctgg ccgcagagat ggcagcagca ttcctcaatg aaaacctccc 1860 tgaatccatc tttggagctc ccaaggctgg caatgggcag tgggcctctg tgatccgagt 1920 gatgaatccc attcaaggga acacactgga ccttgtccag ctggaacaga atgaggcagc 1980 ttttagtgtg gctgtgtgca ggttttccaa cactggtgaa gactggtatg tgctggtggg 2040 tgtggccaag gacctgatac taaacccccg atctgtggca gggggcttcg tctatactta 2100 caagcttgtg aacaatgggg aaaaactgga gtttttgcac aagactcctg tggaagaggt 2160 ccctgctgct attgccccat tccaggggag ggtgttgatt ggtgtgggga agctgttgcg 2220 tgtctatgac ctgggaaaga agaagttact ccgaaaatgt gagaataagc atattgccaa 2280 ttatatctct gggatccaga ctattggaca tagggtaatt gtatctgatg tccaagaaag 2340 tttcatctgg gttcgctaca agcgtaatga aaaccagctt atcatctttg ctgatgatac 2400 ctacccccga tgggtcacta cagccagcct cttggactat gacactgtgg ctggggcaga 2460 caagtttggc aacatatgtg tggtgaggct cccacctaac accaatgatg aagtagatga 2520 ggatcctaca ggaaacaaag ccctgtggga ccgtggcttg ctcaatgggg cctcccagaa 2580 ggcagaggtg atcatgaatt accatgtcgg ggagacggtg ctgtccttgc agaagaccac 2640 gctgatccct ggaggctcag aatcacttgt ctataccacc ttgtctggag gaattggcat 2700 ccttgtgcca ttcacgtccc atgaggacca tgacttcttc cagcatgtgg aaatgcacct 2760 gcggtctgaa catccccctc tctgtgggcg ggaccacctc agctttcgct cctactactt 2820 ccctgtgaag aatgtgattg atggagacct ctgtgagcag ttcaattcca tggaacccaa 2880 caaacaaaag aacgtctctg aagaactgga ccgaacccca cccgaagtgt ccaagaaact 2940 cgaggatatc cggacccgct acgccttctg agccctcctt tcccggtggg gcttgccaga 3000 gactgtgtgt tttgtttccc ccaccaccat castgccacc tggcttctgc catgtggcag 3060 gagggtgact ggataattaa gastgcatta tgaaagtcaa cagctctttc ccctcagctc 3120 ttctcstgga atgactggct tcccctcaaa ttggcactga gatttgctac acttctcccc 3180 acctggtaca tgatacatga ccccaggttc cagtgtagaa cctgagtccc ccattcccca 3240 aagccatccc tgcattgata tgtcttgact ctcctgtcta cttttgcaca cacccttaat 3300 ttttaattgg ttttcttgta aatacaaaaa aaaaaaaaaa 3340 <210> SEQ ID NO 22 <211> LENGTH: 933 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 22 Met Ile Phe Val Cys Ser Ala Thr His Lys Thr Lys Ser Met Phe Phe 1 5 10 15 Phe Leu Ala Gln Thr Glu Gln Gly Asp Ile Phe Lys Ile Thr Leu Glu 20 25 30 Thr Asp Glu Asp Met Val Thr Glu Ile Arg Leu Lys Tyr Phe Asp Thr 35 40 45 Val Pro Val Ala Ala Ala Met Cys Val Leu Lys Thr Gly Phe Leu Phe 50 55 60 Val Ala Ser Glu Phe Gly Asn His Tyr Leu Tyr Gln Ile Ala His Leu 65 70 75 80 Gly Asp Asp Asp Glu Glu Pro Glu Phe Ser Ser Ala Met Pro Leu Glu 85 90 95 Glu Gly Asp Thr Phe Phe Phe Gln Pro Arg Pro Leu Lys Asn Leu Val 100 105 110 Leu Val Asp Glu Leu Asp Ser Leu Ser Pro Ile Leu Phe Cys Gln Ile 115 120 125 Ala Asp Leu Ala Asn Glu Asp Thr Pro Gln Leu Tyr Val Ala Cys Gly 130 135 140 Arg Gly Pro Arg Ser Ser Leu Arg Val Leu Arg His Gly Leu Glu Val 145 150 155 160 Ser Glu Met Ala Val Ser Glu Leu Pro Gly Asn Pro Asn Ala Val Trp 165 170 175 Thr Val Arg Arg His Ile Glu Asp Glu Phe Asp Ala Tyr Ile Ile Val 180 185 190 Ser Phe Val Asn Ala Thr Leu Val Leu Ser Ile Gly Glu Thr Val Glu 195 200 205 Glu Val Thr Asp Ser Gly Phe Leu Gly Thr Thr Pro Thr Leu Ser Cys 210 215 220 Ser Leu Leu Gly Asp Asp Ala Leu Val Gln Val Tyr Pro Asp Gly Ile 225 230 235 240 Arg His Ile Arg Ala Asp Lys Arg Val Asn Glu Trp Lys Thr Pro Gly 245 250 255 Lys Lys Thr Ile Val Lys Cys Ala Val Asn Gln Arg Gln Val Val Ile 260 265 270 Ala Leu Thr Gly Gly Glu Leu Val Tyr Phe Glu Met Asp Pro Ser Gly 275 280 285 Gln Leu Asn Glu Tyr Thr Glu Arg Lys Glu Met Ser Ala Asp Val Val 290 295 300 Cys Met Ser Leu Ala Asn Val Pro Pro Gly Glu Gln Arg Ser Arg Phe 305 310 315 320 Leu Ala Val Gly Leu Val Asp Asn Thr Val Arg Ile Ile Ser Leu Asp 325 330 335 Pro Ser Asp Cys Leu Gln Pro Leu Ser Met Gln Ala Leu Pro Ala Gln 340 345 350 Pro Glu Ser Leu Cys Ile Val Glu Met Gly Gly Thr Glu Lys Gln Asp 355 360 365 Glu Leu Gly Glu Arg Gly Ser Ile Gly Phe Leu Tyr Leu Asn Ile Gly 370 375 380 Leu Gln Asn Gly Val Leu Leu Arg Thr Val Leu Asp Pro Val Thr Gly 385 390 395 400 Asp Leu Ser Asp Thr Arg Thr Arg Tyr Leu Gly Ser Arg Pro Val Lys 405 410 415 Leu Phe Arg Val Arg Met Gln Gly Gln Glu Ala Val Leu Ala Met Ser 420 425 430 Ser Arg Ser Trp Leu Ser Tyr Ser Tyr Gln Ser Arg Phe His Leu Thr 435 440 445 Pro Leu Ser Tyr Glu Thr Leu Glu Phe Ala Ser Gly Phe Ala Ser Glu 450 455 460 Gln Cys Pro Glu Gly Ile Val Ala Ile Ser Thr Asn Thr Leu Arg Ile 465 470 475 480 Leu Ala Leu Glu Lys Leu Gly Ala Val Phe Asn Gln Val Ala Phe Pro 485 490 495 Leu Gln Tyr Thr Pro Arg Lys Phe Val Ile His Pro Glu Ser Asn Asn 500 505 510 Leu Ile Ile Ile Glu Thr Asp His Asn Ala Tyr Thr Glu Ala Thr Lys 515 520 525 Ala Gln Arg Lys Gln Gln Met Ala Glu Glu Met Val Glu Ala Ala Gly 530 535 540 Glu Asp Glu Arg Glu Leu Ala Ala Glu Met Ala Ala Ala Phe Leu Asn 545 550 555 560 Glu Asn Leu Pro Glu Ser Ile Phe Gly Ala Pro Lys Ala Gly Asn Gly 565 570 575 Gln Trp Ala Ser Val Ile Arg Val Met Asn Pro Ile Gln Gly Asn Thr 580 585 590 Leu Asp Leu Val Gln Leu Glu Gln Asn Glu Ala Ala Phe Ser Val Ala 595 600 605 Val Cys Arg Phe Ser Asn Thr Gly Glu Asp Trp Tyr Val Leu Val Gly 610 615 620 Val Ala Lys Asp Leu Ile Leu Asn Pro Arg Ser Val Ala Gly Gly Phe 625 630 635 640 Val Tyr Thr Tyr Lys Leu Val Asn Asn Gly Glu Lys Leu Glu Phe Leu 645 650 655 His Lys Thr Pro Val Glu Glu Val Pro Ala Ala Ile Ala Pro Phe Gln 660 665 670 Gly Arg Val Leu Ile Gly Val Gly Lys Leu Leu Arg Val Tyr Asp Leu 675 680 685 Gly Lys Lys Lys Leu Leu Arg Lys Cys Glu Asn Lys His Ile Ala Asn 690 695 700 Tyr Ile Ser Gly Ile Gln Thr Ile Gly His Arg Val Ile Val Ser Asp 705 710 715 720 Val Gln Glu Ser Phe Ile Trp Val Arg Tyr Lys Arg Asn Glu Asn Gln 725 730 735 Leu Ile Ile Phe Ala Asp Asp Thr Tyr Pro Arg Trp Val Thr Thr Ala 740 745 750 Ser Leu Leu Asp Tyr Asp Thr Val Ala Gly Ala Asp Lys Phe Gly Asn 755 760 765 Ile Cys Val Val Arg Leu Pro Pro Asn Thr Asn Asp Glu Val Asp Glu 770 775 780 Asp Pro Thr Gly Asn Lys Ala Leu Trp Asp Arg Gly Leu Leu Asn Gly 785 790 795 800 Ala Ser Gln Lys Ala Glu Val Ile Met Asn Tyr His Val Gly Glu Thr 805 810 815 Val Leu Ser Leu Gln Lys Thr Thr Leu Ile Pro Gly Gly Ser Glu Ser 820 825 830 Leu Val Tyr Thr Thr Leu Ser Gly Gly Ile Gly Ile Leu Val Pro Phe 835 840 845 Thr Ser His Glu Asp His Asp Phe Phe Gln His Val Glu Met His Leu 850 855 860 Arg Ser Glu His Pro Pro Leu Cys Gly Arg Asp His Leu Ser Phe Arg 865 870 875 880 Ser Tyr Tyr Phe Pro Val Lys Asn Val Ile Asp Gly Asp Leu Cys Glu 885 890 895 Gln Phe Asn Ser Met Glu Pro Asn Lys Gln Lys Asn Val Ser Glu Glu 900 905 910 Leu Asp Arg Thr Pro Pro Glu Val Ser Lys Lys Leu Glu Asp Ile Arg 915 920 925 Thr Arg Tyr Ala Phe 930 <210> SEQ ID NO 23 <211> LENGTH: 1496 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 23 gccagcccca ccgctgaccc agagcttgga actgaggagc cccaggcagg gagttgatgg 60 gaccccgaaa gaaagtgtgg gatggagggt ctagccccgg gcagctgcgg ctcartgggc 120 agcsggaccc cgggaggagg aggcggcacc tccgccccac agcctcaccc ggcccttccc 180 tcccgctcac ttggctgcaa gccagtgtcc tccgtggtga gccggccctt gctgctctgc 240 atgatcaggc tcgggaacct gaggtcagcc atgctgtgct ccggcagccc ctgcctgcct 300 cctcgcggag cccttctgcc ccttgggctg cstgtgccgg ggcgaggcct gtgtggggcc 360 tgtgatggca gctcctggaa aacgctgtgg ggcaggggtg aggcccacga ggccatgggg 420 acagctcacc atggggagca cacctgcagg tggggagggc tgcctttccc cacagcactc 480 agaagatgca cgtggccggg gctgatgagc tgccccgagc cacccctggg ggtcactgag 540 ggcagggctg gcagcacaga tgcccctgct cggggcctga gtggggccag cgctgacagg 600 ctgtcctctc gtcctctttt tcatggcggc ggtccttctt cagatgacga cgccggctct 660 gcacccctga agagcagcgg gcagcaccag aatgacaaag gcaagaacgt ccgccagagg 720 aactcttcct gaggcaggtg gcccgaggac gctccctgct ccgcgtctgc gccgccgccg 780 gagtccactc ccagtgcttg caagattcca agttctcacc tcttaaagaa aacccacccc 840 gtagattccc atcatacact tccttctttt ttaaaaaagt tgggttttct ccattcagga 900 ttctgttcct taggattttt tccttctgaa gtgtttcacg agagcccggg agctgctgcc 960 ctgcggcccc gtctgtggct ttcagcctct gggtctgagt catggccggg tgggcggcac 1020 agccttctcc actggccgga gtcagtgcca ggtccttgcc ctttgtggaa agtcacaggt 1080 cacacgaggg gccccgtgtc ctgcctgtct gaagccaatg ctgtctggtt gcgccatttt 1140 tgtgctttta tgtttaattt tatgagggcc acgggtctgt gttcgactca gcctcaggga 1200 cgactctgac ctcttggcca cagaggactc acttgcccac accgagggcg accccgtcac 1260 agcctcaagt cactcccaag ccccctcctt gtctgtgcat ccgggggcag ctctggaggg 1320 ggtttgctgg ggaactggcg ccatcgccgg gactccagaa ccgcagaagc ctccccagct 1380 cacccctgga ggacggccgg ctctctatag caccagggct cacgtgggaa cccccctccc 1440 acccaccgcc acaataaaga tcgcccccac ctccaccctc aaaaaaaaaa aaaaaa 1496 <210> SEQ ID NO 24 <211> LENGTH: 216 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (12) <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (15) <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (84) <400> SEQUENCE: 24 Met Glu Gly Leu Ala Pro Gly Ser Cys Gly Ser Xaa Gly Ser Xaa Thr 1 5 10 15 Pro Gly Gly Gly Gly Gly Thr Ser Ala Pro Gln Pro His Pro Ala Leu 20 25 30 Pro Ser Arg Ser Leu Gly Cys Lys Pro Val Ser Ser Val Val Ser Arg 35 40 45 Pro Leu Leu Leu Cys Met Ile Arg Leu Gly Asn Leu Arg Ser Ala Met 50 55 60 Leu Cys Ser Gly Ser Pro Cys Leu Pro Pro Arg Gly Ala Leu Leu Pro 65 70 75 80 Leu Gly Leu Xaa Val Pro Gly Arg Gly Leu Cys Gly Ala Cys Asp Gly 85 90 95 Ser Ser Trp Lys Thr Leu Trp Gly Arg Gly Glu Ala His Glu Ala Met 100 105 110 Gly Thr Ala His His Gly Glu His Thr Cys Arg Trp Gly Gly Leu Pro 115 120 125 Phe Pro Thr Ala Leu Arg Arg Cys Thr Trp Pro Gly Leu Met Ser Cys 130 135 140 Pro Glu Pro Pro Leu Gly Val Thr Glu Gly Arg Ala Gly Ser Thr Asp 145 150 155 160 Ala Pro Ala Arg Gly Leu Ser Gly Ala Ser Ala Asp Arg Leu Ser Ser 165 170 175 Arg Pro Leu Phe His Gly Gly Gly Pro Ser Ser Asp Asp Asp Ala Gly 180 185 190 Ser Ala Pro Leu Lys Ser Ser Gly Gln His Gln Asn Asp Lys Gly Lys 195 200 205 Asn Val Arg Gln Arg Asn Ser Ser 210 215 <210> SEQ ID NO 25 <211> LENGTH: 2113 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 25 gcagctatgg ctgctggcgt accctgtgcg ttagtcacca gctgctcctc cgtcttctca 60 ggagaccagc tggtccaaca tatccttgga acagaagatc ttattgtgga agtgacttcc 120 aatgatgctg tgagatttta tccctggacc attgataata aatactattc agcagacatc 180 aatctatgtg tggtgccaaa caaatttctt gttactgcag agattgcaga atctgtccaa 240 gcatttgtgg tttactttga cagcacacaa aaatcgggcc ttgatagtgt ctcctcrtgg 300 cttccactgg caaaagcatg gttacctgag gtgatgatct tggtctgcga tagagtgtct 360 gaagatggta taaaccgaca aaaagctcaa gaatggtgcc tcaaacatgg ctttgaattg 420 gtagaactta gtccagagga gttgcctgag gaggatgatg acttcccaga atctacagga 480 gtaaagcgaa ttgtccaagc cctgaatgcc aatgtgtggt ccaatgtagt gatgaagaat 540 gataggaacc aaggctttag ccttctcaac tcattgactg gaacaaacca tagcattggg 600 tcagcagatc cctgtcaccc agagcaaccc catttgccag cagcagatag tactgaatcc 660 ctctctgatc atcggggtgg tgcatctaac acaacagatg cccaggttga tagcattgtg 720 gatcccatgt tagatctgga tattcaagaa ttagccagtc ttaccactgg aggaggagat 780 gtggagaatt ttgaaagact cttttcaaag ttaaaggaaa tgaaagacaa ggctgcgacg 840 cttcctcatg agcaaagaaa agtgcatgca gaaaaggtgg ccaaagcatt ctggatggca 900 atcgggggag acagagatga aattgaaggc ctttcatctg atgaagagca ctgaattatt 960 catactaggg tttgaccaac aaagatgcta gctgtctctg agatacctct ctactcagcc 1020 cagtcatatt ttgccaaaat tgcccttatc atgttggctg cctgacttgt ttatagggtc 1080 cccttaattt tagtttttag taggaggtta aggagaaatc ttttttttcc tcagtatatt 1140 gtaagagagt gaggaataca gtgatagtaa tgagtgagga tttcttaaat gtactttttt 1200 tttgttctag gaatgagggt aggataaatc tcagaggtct gtgtgattta ctcaagttga 1260 agacaacctc caggccattc ctggtcaacg ttttaagtag catttccagc attcacactt 1320 gatactgcac atcaggagtt gtgtcacctt tcctgggtga tttgggtttt ctccattcaa 1380 ggagcttgta gctctgagct atgatgcttt tattgggagg aaaggaggca gctgcagaat 1440 tgatgtgagc tatgtggggc cgaagtctca gcccgcagct aagtctctac ctaagaaaat 1500 gcctctgggc attcttttga agtatagtgt ctgagctcat gctagaaaga atcaaaaagc 1560 cagtgtggat ttttagactg taataaatga ggcaaaggat ttctattcca gtgggaagaa 1620 aacctctcta ctgagttgtg ggggatatgt tgtatgttag agagaacctt aaggagtcct 1680 tgtatgggcc atggagacag tatgtgataa cataccgtga ttttcatgaa gaaattcttc 1740 tgtcttagag ttctcccctg ctgcttgaga tgccagagct gtgttgttgc acacctgcaa 1800 aacaaggcac atttccccct ttctctttaa agccaaagag agatcactgc caaagtggga 1860 gcactaaggg gtgggtgggg aagtgaaatg ttaggcgatg aattcctgag caccttgttt 1920 ttcttccaag gttcgtagct tctctctgcc cttccaagcc tgtaacctcg gaggactatc 1980 ttttgttctt tatcctttgt cttgttwgag tgggtcagcc ccagaggaac tgataagcaa 2040 atggcaagtt tttaaaggaa gagtggaaag tactgcaaat aaaaatcctt atttgttaaa 2100 aaaaaaaaaa aaa 2113 <210> SEQ ID NO 26 <211> LENGTH: 315 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 26 Met Ala Ala Gly Val Pro Cys Ala Leu Val Thr Ser Cys Ser Ser Val 1 5 10 15 Phe Ser Gly Asp Gln Leu Val Gln His Ile Leu Gly Thr Glu Asp Leu 20 25 30 Ile Val Glu Val Thr Ser Asn Asp Ala Val Arg Phe Tyr Pro Trp Thr 35 40 45 Ile Asp Asn Lys Tyr Tyr Ser Ala Asp Ile Asn Leu Cys Val Val Pro 50 55 60 Asn Lys Phe Leu Val Thr Ala Glu Ile Ala Glu Ser Val Gln Ala Phe 65 70 75 80 Val Val Tyr Phe Asp Ser Thr Gln Lys Ser Gly Leu Asp Ser Val Ser 85 90 95 Ser Trp Leu Pro Leu Ala Lys Ala Trp Leu Pro Glu Val Met Ile Leu 100 105 110 Val Cys Asp Arg Val Ser Glu Asp Gly Ile Asn Arg Gln Lys Ala Gln 115 120 125 Glu Trp Cys Leu Lys His Gly Phe Glu Leu Val Glu Leu Ser Pro Glu 130 135 140 Glu Leu Pro Glu Glu Asp Asp Asp Phe Pro Glu Ser Thr Gly Val Lys 145 150 155 160 Arg Ile Val Gln Ala Leu Asn Ala Asn Val Trp Ser Asn Val Val Met 165 170 175 Lys Asn Asp Arg Asn Gln Gly Phe Ser Leu Leu Asn Ser Leu Thr Gly 180 185 190 Thr Asn His Ser Ile Gly Ser Ala Asp Pro Cys His Pro Glu Gln Pro 195 200 205 His Leu Pro Ala Ala Asp Ser Thr Glu Ser Leu Ser Asp His Arg Gly 210 215 220 Gly Ala Ser Asn Thr Thr Asp Ala Gln Val Asp Ser Ile Val Asp Pro 225 230 235 240 Met Leu Asp Leu Asp Ile Gln Glu Leu Ala Ser Leu Thr Thr Gly Gly 245 250 255 Gly Asp Val Glu Asn Phe Glu Arg Leu Phe Ser Lys Leu Lys Glu Met 260 265 270 Lys Asp Lys Ala Ala Thr Leu Pro His Glu Gln Arg Lys Val His Ala 275 280 285 Glu Lys Val Ala Lys Ala Phe Trp Met Ala Ile Gly Gly Asp Arg Asp 290 295 300 Glu Ile Glu Gly Leu Ser Ser Asp Glu Glu His 305 310 315 <210> SEQ ID NO 27 <211> LENGTH: 1541 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 27 ttaaaagaca aaattttaaa atctgacccc agcccttgtg attgttcagt atataatcaa 60 tggtatctta caaggactat tttatttgga atcaatcaaa tttgtttcct gccaacaata 120 agttaggttg ttttttgcag ttctcaagta acaaatatga ggaccgaact ctcattcaac 180 atccaagccc ttgcagtttg tgcaaatata tgtttagcaa caaaggacag acagaatcca 240 tcattagtat ggctttttac tggaatgttt tgcatttatt cattgttctt tgcttggaga 300 gcaaatttag atatttcaaa accacttttc atgggtgtgg tggaacgatt ctggatgcag 360 agcaatgcag tagtggccgt cctcgctggc attggtttgg ctgcagttgt gtctgagact 420 aaccgagtgc tgaatagcaa tgggcttcag tgtctggaat ggctttctgc mactcttttt 480 gtagtttacc aaatatattc taattacaga aaagaaacat ttgtttgcat aggaattcat 540 gaaggcgacc caacctggaa aaagaactat tcactttggc catgggggtc ttgtgacaaa 600 ttagttcctt tggagattgt attcaaccct gaggaatgga ttaaacttac aaaaaatatc 660 tataactgga ccgaagaata tggaaggttt gatccatctt cttgggaatc tgtggccaat 720 gaagaaatgt ggcaagcgag gatgaaaaca ccgttcttca tctttaacct ggcagaaact 780 gctcacatgc cttcaaaagt gaaagctcaa ctctacgctc aagcatatga cctttataag 840 gagattgtct atttacaaaa ggagcaccca gtgaattggc acaagaacta tgccatcgcc 900 tgtgagcgga tgctgcgtct tcaggcaaga gatgcagatc ctgaagtgct gttatcggaa 960 accatcagac atttccgtct gtactctcag aaagcaccga atgacccaca gcaagctgat 1020 attttaggtg ctctaaagca cctaagaaaa gaactgcaaa gtctgagaaa taggaaaaat 1080 gtctgagaca gcaaaatatg aaaaacctgc tcatcgttca gcttccaaaa ttctgaagtc 1140 tggaagtttt tccttcaaag aaaagaaact gcataaaaaa tttaaaacta agtcatctcc 1200 cagatataag tatcatggtc cagcagtact gtttaatggg gtattcagtg actaaggtct 1260 gctatttatg caaaattctg tttatcccgt gttaccaaat taccatttca gtgagaagct 1320 tttgaaaagt cttctgactt ccagtctttc accagatgac tgcactggat tagattctag 1380 aagagaatga accattttca tataactaaa tattggtcat gaactgtgta agggccatgc 1440 ttattgggat cagttttaaa gttaaattct tttgatatta ataccagacc aaagacattt 1500 tctgtttcct gaaaaaaaaa aaaaaaaaaa aaaaaaaaaa a 1541 <210> SEQ ID NO 28 <211> LENGTH: 309 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 28 Met Arg Thr Glu Leu Ser Phe Asn Ile Gln Ala Leu Ala Val Cys Ala 1 5 10 15 Asn Ile Cys Leu Ala Thr Lys Asp Arg Gln Asn Pro Ser Leu Val Trp 20 25 30 Leu Phe Thr Gly Met Phe Cys Ile Tyr Ser Leu Phe Phe Ala Trp Arg 35 40 45 Ala Asn Leu Asp Ile Ser Lys Pro Leu Phe Met Gly Val Val Glu Arg 50 55 60 Phe Trp Met Gln Ser Asn Ala Val Val Ala Val Leu Ala Gly Ile Gly 65 70 75 80 Leu Ala Ala Val Val Ser Glu Thr Asn Arg Val Leu Asn Ser Asn Gly 85 90 95 Leu Gln Cys Leu Glu Trp Leu Ser Ala Thr Leu Phe Val Val Tyr Gln 100 105 110 Ile Tyr Ser Asn Tyr Arg Lys Glu Thr Phe Val Cys Ile Gly Ile His 115 120 125 Glu Gly Asp Pro Thr Trp Lys Lys Asn Tyr Ser Leu Trp Pro Trp Gly 130 135 140 Ser Cys Asp Lys Leu Val Pro Leu Glu Ile Val Phe Asn Pro Glu Glu 145 150 155 160 Trp Ile Lys Leu Thr Lys Asn Ile Tyr Asn Trp Thr Glu Glu Tyr Gly 165 170 175 Arg Phe Asp Pro Ser Ser Trp Glu Ser Val Ala Asn Glu Glu Met Trp 180 185 190 Gln Ala Arg Met Lys Thr Pro Phe Phe Ile Phe Asn Leu Ala Glu Thr 195 200 205 Ala His Met Pro Ser Lys Val Lys Ala Gln Leu Tyr Ala Gln Ala Tyr 210 215 220 Asp Leu Tyr Lys Glu Ile Val Tyr Leu Gln Lys Glu His Pro Val Asn 225 230 235 240 Trp His Lys Asn Tyr Ala Ile Ala Cys Glu Arg Met Leu Arg Leu Gln 245 250 255 Ala Arg Asp Ala Asp Pro Glu Val Leu Leu Ser Glu Thr Ile Arg His 260 265 270 Phe Arg Leu Tyr Ser Gln Lys Ala Pro Asn Asp Pro Gln Gln Ala Asp 275 280 285 Ile Leu Gly Ala Leu Lys His Leu Arg Lys Glu Leu Gln Ser Leu Arg 290 295 300 Asn Arg Lys Asn Val 305 <210> SEQ ID NO 29 <211> LENGTH: 539 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (495) <400> SEQUENCE: 29 gcgggccgga gggtgatggg accatctagc ccctaaccat gggcccagaa gagaagacca 60 tcatgacaga taggtctgca gctgttttca tccaggcctg gtggcggggc atgctggtgc 120 gacgacactg ctgcatgcag ccctcagggc ttggttcatt cagtgctggt ggaggcaggt 180 gctggagaag ctgctggcaa agaggcggag gatggtgttg gagttctatg tgcagcagga 240 atgggcagca gtcaggctgc agtcctgggt ccgcatgtgg tgtgtccgcc agcgtaactg 300 ttgtttgctc aacgctgtcc gcatcatcca ggtctattgg cgctggcaca gctgccattc 360 ccgtggcaaa attgagggcc actatgaact caaaaaaaac caacaaaaaa aacaacatga 420 aaacaccttg ggctaacagg cttgtaaggt gcaacaatgc ataccccttc cattaaaaaa 480 atgaccaggt ctgcnaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaa 539 <210> SEQ ID NO 30 <211> LENGTH: 145 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 30 Met Gly Pro Glu Glu Lys Thr Ile Met Thr Asp Arg Ser Ala Ala Val 1 5 10 15 Phe Ile Gln Ala Trp Trp Arg Gly Met Leu Val Arg Arg His Cys Cys 20 25 30 Met Gln Pro Ser Gly Leu Gly Ser Phe Ser Ala Gly Gly Gly Arg Cys 35 40 45 Trp Arg Ser Cys Trp Gln Arg Gly Gly Gly Trp Cys Trp Ser Ser Met 50 55 60 Cys Ser Arg Asn Gly Gln Gln Ser Gly Cys Ser Pro Gly Ser Ala Cys 65 70 75 80 Gly Val Ser Ala Ser Val Thr Val Val Cys Ser Thr Leu Ser Ala Ser 85 90 95 Ser Arg Ser Ile Gly Ala Gly Thr Ala Ala Ile Pro Val Ala Lys Leu 100 105 110 Arg Ala Thr Met Asn Ser Lys Lys Thr Asn Lys Lys Asn Asn Met Lys 115 120 125 Thr Pro Trp Ala Asn Arg Leu Val Arg Cys Asn Asn Ala Tyr Pro Phe 130 135 140 His 145 <210> SEQ ID NO 31 <211> LENGTH: 2408 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 31 cacatctcag agcctaagaa ataggactaa gcccagaact cctagaatca cctataaatg 60 ctaggcatag atggaaatta ttgtgttcca ccagaagcac agctccaaac tatacctaaa 120 aaatatttct gcacttccca gagacctgga cttcaaactt tcccagtgga gcctgattat 180 agaacttgag ggtcctatct caggatgaag gggagaggcc ctggcttcac gggaaggtat 240 tccagcattg ttctgcttca cccttgactg cgttgtctgg cagtttctgt gtgctgccag 300 gatattatat ggaactggag aagttggagt caggtctctg aagctagagt ttcactaatt 360 agatgcctct gtacatgaga actattactg tctgcaggtc catatagcta agctgccagg 420 aaaaacacat tatcttccaa aactttcaga gcatgtgcag aaccctttct tagcgttttc 480 ttctcagcat tttctctgcc tcccagaggc tggcagccag tgacactgca gagttcagca 540 tgttctaacc atgcacgcag ggcaggggct gccttggccc tcctcaggct ttcgttggga 600 gagcaggcag tggtggagcc cttctgggtg cagtcctctg gggttgctct ttggaactca 660 tgtatgagtt tgactccaca aggcttggca tggataccaa aacagttgca acaaattagt 720 tctgaacctg gaacagagaa ttcagtgctt ctgttactca ggaaggaggt gttcagaatg 780 ccccgtgcag agcagccagt cattactctt gtttgttctc acctgggtgc gcaccctcat 840 gatgcagtgg ctgtagcacc ttcatgccag gtgctgagag aatgggaaat tcttcctccc 900 cattgacctg agtcccagag acttagggac acagacttca ggtgaggctg cggacctcag 960 aagcagtgga taatagattg gggcattaaa agcttttgag gcagggggct catgttttga 1020 ctgcagggag ttatgctgag caaagagatg tgtttttcaa aaccagggtt caaaaccagt 1080 gtccacgctg gagtaagtgg agcatgcttc tctgtgttct ctgaatgatc ttgcactcct 1140 cttaagcaaa ggagtaccat gaccatagtc agtgggatcc cacaaatgtt cttaaatggg 1200 taaggcttta agtagccaga gagtatccag cctaccattg gcttctccac atcctaaaac 1260 ctgagacagc cttggtatat gctttataaa tgtttctttt cttgttgttt aagtaattaa 1320 agtgtttaaa atgtcttcat tagatgtgac gattgtttaa tgagtttgcc tctgacgtgt 1380 ggctccatgg gagataggca aagtaattaa gaagttacca gaaattggtc ggctggggaa 1440 atgcaaaagt tagcatttca gtagtgaatt tctcctggaa caaatgagca atttttcctc 1500 tttctcttaa gtagtatacc cttttctcac ttagtaattt aatggtatat aaagacatgt 1560 gtataagtga gtgcatacat atgaggtatg actatagggt tgtttgtggg aatttctttt 1620 cctaacatac agaagatcaa agtgttcatc tcaccccgcc ctccttaaaa ggtgtctttt 1680 gggagactat gtgctcattg actatagtgc tgccaagtaa aatatcttgg gaactcttct 1740 actagaatgg ccttcagggc ttggcatgtt cctttggttt acccttagag atgagaaatc 1800 ctcctccttt gaggatggat ttaagttctg gaaataatct caagtgcttg atagcacagt 1860 tggatgaaaa aagatggcaa ttaaggtaag ttacaccatt tttgtttcta aaaaaatccc 1920 taagaaattt cttggaatga gtctttggcc tcagagcctc tcaaagtgtc cacttcaagg 1980 ggggatcatc ctcattagca cacagatttt taaaaatcaa ttctcttgcc atgcctccta 2040 tgtgttcaca tctctgcata cactacagat ataagtgcat aatcattcat ataaacatct 2100 ggtaggtatt ctgtaaaact gtgtttactt tagtgcatgt tattgtcatg ttatgatgtg 2160 actggggtgt ttctttgtca tgaaactttg cttcttcaca gaattagaat actgctctct 2220 ctatattgaa ctacatatac agcgttttct tgtatcagcc cccaaagtct ggatgcccgg 2280 tgttgtgttt acatgtgatt gtgcctagga gtctgttcac atagagacac ctgtaagtat 2340 ttattacaaa acggaatgta agcaaatata tccacattgg ttttatttga aaaaaaaaaa 2400 aaaaaaaa 2408 <210> SEQ ID NO 32 <211> LENGTH: 80 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 32 Met Ser Leu Thr Pro Gln Gly Leu Ala Trp Ile Pro Lys Gln Leu Gln 1 5 10 15 Gln Ile Ser Ser Glu Pro Gly Thr Glu Asn Ser Val Leu Leu Leu Leu 20 25 30 Arg Lys Glu Val Phe Arg Met Pro Arg Ala Glu Gln Pro Val Ile Thr 35 40 45 Leu Val Cys Ser His Leu Gly Ala His Pro His Asp Ala Val Ala Val 50 55 60 Ala Pro Ser Cys Gln Val Leu Arg Glu Trp Glu Ile Leu Pro Pro His 65 70 75 80 <210> SEQ ID NO 33 <211> LENGTH: 970 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 33 gtgcgagatt gaggaagggt cggggcttaa cgggggaggt gggggtggcg gggggggaac 60 agcacggcgc ggcgcctagc ctgcgagatg gagtcggagt gggggtgcga gcggtcctcc 120 accgcctctg cccgatccgt acctcacaat ggactgctcg agtttgtatc taggcctgtc 180 caggattgtt tactccttca attaatcagc tttatctctt ttccccctcc ccccacctcc 240 accaaatctg gagaggagtg ggaaagaact ggaaaactca cagggcaaag agagaaagcc 300 aacagtcata gtgcgggagg aggcacgcct gggatgcaat acccaacagt ctcctccctg 360 ctttcctgca atttgcaggt cattgtcttt cttatttgta gctttttttt tttttcttca 420 gtagccggta aacaatcgaa cgacgggtag ggaggtcaga ggggatgggg ctgtgggaga 480 gattctactc aggctaggtg ctttagattt ggacctggct gtgtccctac tttattaaaa 540 ttctcatgtg gcgcgcgctg tcttctctct tctctctctc tctctctcac acacacacgc 600 acatacacac acagcccgag agaaatttcc aatcctttga gcaaatctct tccatctagt 660 ccttgaaaca gaggaaagga catgggacct gaaggagagt tatgattgaa ttttctaaaa 720 tttagttttg acattgcaaa gtaaaagtga ggaccgtatt cccaatacag acccagaggg 780 tggttatttc aggtgagggg acctcagcct gtgacgtcta tgatcaacca gacaaagacc 840 ccttcctaaa tctgaagtcc cacccccacc cgtggcaaac atggaataca agggagggga 900 aggatggcac aatagtgggt tctgttttcc aagaactgcc ccccacctcc attgcaaaaa 960 aaaaaaaaaa 970 <210> SEQ ID NO 34 <211> LENGTH: 120 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 34 Met Glu Ser Glu Trp Gly Cys Glu Arg Ser Ser Thr Ala Ser Ala Arg 1 5 10 15 Ser Val Pro His Asn Gly Leu Leu Glu Phe Val Ser Arg Pro Val Gln 20 25 30 Asp Cys Leu Leu Leu Gln Leu Ile Ser Phe Ile Ser Phe Pro Pro Pro 35 40 45 Pro Thr Ser Thr Lys Ser Gly Glu Glu Trp Glu Arg Thr Gly Lys Leu 50 55 60 Thr Gly Gln Arg Glu Lys Ala Asn Ser His Ser Ala Gly Gly Gly Thr 65 70 75 80 Pro Gly Met Gln Tyr Pro Thr Val Ser Ser Leu Leu Ser Cys Asn Leu 85 90 95 Gln Val Ile Val Phe Leu Ile Cys Ser Phe Phe Phe Phe Ser Ser Val 100 105 110 Ala Gly Lys Gln Ser Asn Asp Gly 115 120 <210> SEQ ID NO 35 <211> LENGTH: 2084 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 35 ggtagccgtt gggttgggaa agtgagggat ttttggcctc gtttctcctg cttcttttct 60 cctccctttt actttgccgg tagaacacag ttatgggtcg caagaagaag aagcagctga 120 agccgtggtg ctggtattgt catagagatt ttgatgatga gaagatcctt attcagcacc 180 aaaaagcaaa gcattttaaa tgccatatat gtcacaagaa attgtataca ggacctggct 240 tagctattca ttgcatgcag gtacataaag aaacaataga tgccgtacca aatgcaatac 300 ctggaagaac agacatagag ttggaaatat atggtatgga aggtattcca gaaaaagaca 360 tggatgaaag acgacgactt cttgaacaga aaacacaaga aagtctaaaa aagaagcaac 420 aagatgattc tgatgaatat gatgatgacg actctgcagc ctcaacttca tttcagccac 480 agcctgttca acctcagcaa ggttatattc ctccaatggc acagccagga ctgccaccag 540 taccaggagc accaggaatg cctccaggca tacctccatt aatgccacgt gttcctcctc 600 tgatgccagg aatgccacca gttatgccag gcatgccacc tggattgcat catcagagaa 660 aatacaccca gtcattttgc ggtgaaaaca taatgatgcc aatgggtgga atgatgccac 720 ctggaccagg aataccacct ctgatgcctg gaatgccacc aggtatgccc ccacctgttc 780 cacgtcctgg aattcctcca atgactcaag cacaggctgt ttcagcgcca ggtattctta 840 atagaccacc tgcaccaaca gcaactgtac ctgccccaca gcctccagtt actaagcctc 900 ttttccctag tgctggacag gctcaggcag ctgtccaagg acctgttggt acagatttca 960 aacccttaaa tagtacccct gcaacaacta cagaaccccc aaagcctaca ttccctgctt 1020 atacacagtc tacagcttca acaactagta caacaaatag tactgcagct aaaccagcgg 1080 cttcaataac aagtaagcct gctacactta caacaactag tgcaaccagt aagttgatcc 1140 atccagatga ggatatatcc ctggaagaga gaagggcaca gttacctaag tatcaacgta 1200 atcttcctcg gccaggacag gcccccatcg gtaatccacc agttggacca attggaggta 1260 tgatgccacc acagccaggc atcccacagc aacaaggaat gagaccccca atgccacctc 1320 atggtcagta tggtggtcat catcaaggca tgccaggata ccttcctggt gctatgcccc 1380 cgtatgggca gggaccgcca atggtgcccc cttaccaggg tgggcctcct cgacctccga 1440 tgggaatgag acctcctgta atgtcgcaag gtggccgtta ctgatcttac ttcatccagt 1500 ctaataggtt tggagattaa accttttctc aacttgtgct gtttatatag ccaagcttcc 1560 gtcaataagg cttcattgtg actttaacaa acattctctt cccacatacc aggaactatt 1620 ggacatttat tttacatggg aaaaattatt tggaataata aagcaggaac ttttcctgaa 1680 gttgcaattt atactgtatg gcttcttttt catgtttcat ctaggttttt agaagtgaag 1740 tatagtaaat ttggttcgtt aaattgtgaa ggcgctggaa ttacatgaac ataccaccct 1800 agtaaaggca agttctgtaa gcttacattg ctatttgtaa agtttgcctt cacagcattt 1860 cagatgctgt tggacttcat gtccccaacc tagcttggtg agggctgtaa ctgtttccaa 1920 gtacttgtac attggaagtc tgaatgtgta acaatattta atgtatttag agttcctcat 1980 gttgcagggt ttaagaaatc tgacccacca aggtcatgtg acttttctgt actgttaaac 2040 ttcattgtaa taaaatgaga gaaaaaaaaa aaaaaaaaaa aaaa 2084 <210> SEQ ID NO 36 <211> LENGTH: 463 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 36 Met Gly Arg Lys Lys Lys Lys Gln Leu Lys Pro Trp Cys Trp Tyr Cys 1 5 10 15 His Arg Asp Phe Asp Asp Glu Lys Ile Leu Ile Gln His Gln Lys Ala 20 25 30 Lys His Phe Lys Cys His Ile Cys His Lys Lys Leu Tyr Thr Gly Pro 35 40 45 Gly Leu Ala Ile His Cys Met Gln Val His Lys Glu Thr Ile Asp Ala 50 55 60 Val Pro Asn Ala Ile Pro Gly Arg Thr Asp Ile Glu Leu Glu Ile Tyr 65 70 75 80 Gly Met Glu Gly Ile Pro Glu Lys Asp Met Asp Glu Arg Arg Arg Leu 85 90 95 Leu Glu Gln Lys Thr Gln Glu Ser Leu Lys Lys Lys Gln Gln Asp Asp 100 105 110 Ser Asp Glu Tyr Asp Asp Asp Asp Ser Ala Ala Ser Thr Ser Phe Gln 115 120 125 Pro Gln Pro Val Gln Pro Gln Gln Gly Tyr Ile Pro Pro Met Ala Gln 130 135 140 Pro Gly Leu Pro Pro Val Pro Gly Ala Pro Gly Met Pro Pro Gly Ile 145 150 155 160 Pro Pro Leu Met Pro Arg Val Pro Pro Leu Met Pro Gly Met Pro Pro 165 170 175 Val Met Pro Gly Met Pro Pro Gly Leu His His Gln Arg Lys Tyr Thr 180 185 190 Gln Ser Phe Cys Gly Glu Asn Ile Met Met Pro Met Gly Gly Met Met 195 200 205 Pro Pro Gly Pro Gly Ile Pro Pro Leu Met Pro Gly Met Pro Pro Gly 210 215 220 Met Pro Pro Pro Val Pro Arg Pro Gly Ile Pro Pro Met Thr Gln Ala 225 230 235 240 Gln Ala Val Ser Ala Pro Gly Ile Leu Asn Arg Pro Pro Ala Pro Thr 245 250 255 Ala Thr Val Pro Ala Pro Gln Pro Pro Val Thr Lys Pro Leu Phe Pro 260 265 270 Ser Ala Gly Gln Ala Gln Ala Ala Val Gln Gly Pro Val Gly Thr Asp 275 280 285 Phe Lys Pro Leu Asn Ser Thr Pro Ala Thr Thr Thr Glu Pro Pro Lys 290 295 300 Pro Thr Phe Pro Ala Tyr Thr Gln Ser Thr Ala Ser Thr Thr Ser Thr 305 310 315 320 Thr Asn Ser Thr Ala Ala Lys Pro Ala Ala Ser Ile Thr Ser Lys Pro 325 330 335 Ala Thr Leu Thr Thr Thr Ser Ala Thr Ser Lys Leu Ile His Pro Asp 340 345 350 Glu Asp Ile Ser Leu Glu Glu Arg Arg Ala Gln Leu Pro Lys Tyr Gln 355 360 365 Arg Asn Leu Pro Arg Pro Gly Gln Ala Pro Ile Gly Asn Pro Pro Val 370 375 380 Gly Pro Ile Gly Gly Met Met Pro Pro Gln Pro Gly Ile Pro Gln Gln 385 390 395 400 Gln Gly Met Arg Pro Pro Met Pro Pro His Gly Gln Tyr Gly Gly His 405 410 415 His Gln Gly Met Pro Gly Tyr Leu Pro Gly Ala Met Pro Pro Tyr Gly 420 425 430 Gln Gly Pro Pro Met Val Pro Pro Tyr Gln Gly Gly Pro Pro Arg Pro 435 440 445 Pro Met Gly Met Arg Pro Pro Val Met Ser Gln Gly Gly Arg Tyr 450 455 460 <210> SEQ ID NO 37 <211> LENGTH: 1250 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 37 gtatgttgtc agaccagggt tttcagagtt gatggaaaag agtcttgtga gaaaacttat 60 tttgataaat tattacacac gcagaaaaac tgatcacact gactggatct gtccacgaca 120 tggaaaataa actggatttt cagaatattg ttgttttctg tagtgttcaa ggtattgttt 180 ctaaacataa acatactcta aacatgcttt attcacttgt taaagtcata cttttaaaag 240 taatacctta ctaaagatgg tgattacttt tccgaggtca gaaaaggaaa gctaagcgtt 300 ttcattatca aatacacaag cttattaaat gaatgactgt taactacttt attttcattt 360 gcacattaat tttggaattg tttctgtttt gctgctgacg gaaatactat tttggctctg 420 tgtatatttg tattttgatt tttctggttt gtttaccccc atttgctttt agctccgcct 480 tatgtttaaa tatattctaa cttatgtaaa gagcataatc ttagagcaaa aatacttgag 540 gttttatgtc agatctaatc ttaagtgttt gttgtttttt aaaaggtgtt ttctcagatg 600 gctgcagtgt ttttgctatt tctgcataaa taccctacct ggactcccca gttttcacca 660 gaaactgtta tttttttttg ttgttgttcc cactgagact gatggtgatg gggaaattaa 720 aaacaacaca ctagcacact cccacaaaac ttgaggaaga gttagaatgg caataaaata 780 ttaaatagac cttatactta aaataaggtt tcactatata atttgtcaca attcaatcta 840 atcagctaaa gttaaatgta gttagaatta gccacaggag aatgtaaagc atgctttgac 900 gaagctatcg gtaacacata ttgaatgtct ttgagactct tagattgtac tatttgctta 960 atagattaat gaaatttatc agatacaacc tgtatttcca aaaacaagct agaaggaacc 1020 tgaggaatgt ggtttacatt tgagatccac cttactgtgt tttctacttt cagaaaagat 1080 tctgtagttt tggtttttgg catctttctt atactcagtt ttttctgcct taattcccat 1140 ttaccagcag ttaactcatg tttattgtgc tttcatgcat tgtgatatgg aatgtgttta 1200 gtaatttact ccttataaat atggtaaagt acaaaaaaaa aaaaaaaaaa 1250 <210> SEQ ID NO 38 <211> LENGTH: 90 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 38 Met Phe Lys Tyr Ile Leu Thr Tyr Val Lys Ser Ile Ile Leu Glu Gln 1 5 10 15 Lys Tyr Leu Arg Phe Tyr Val Arg Ser Asn Leu Lys Cys Leu Leu Phe 20 25 30 Phe Lys Arg Cys Phe Leu Arg Trp Leu Gln Cys Phe Cys Tyr Phe Cys 35 40 45 Ile Asn Thr Leu Pro Gly Leu Pro Ser Phe His Gln Lys Leu Leu Phe 50 55 60 Phe Phe Val Val Val Pro Thr Glu Thr Asp Gly Asp Gly Glu Ile Lys 65 70 75 80 Asn Asn Thr Leu Ala His Ser His Lys Thr 85 90 <210> SEQ ID NO 39 <211> LENGTH: 793 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 39 ggcgccttgg aggcgatggc ccacggggct gctagccgtg ctgcggcccc tgctcacctg 60 ccggcccctg caaggcacga cgctgcaacg ggatgtgctg ctctttgagc atgatcgggg 120 ccgcttcttc accatcctcg ggctgttctg cgcgggccag ggcgtcttct gggcttccat 180 ggctgtggca gccgtgtccc ggcccccggt tccggtgcag cctctggatg cggaggtccc 240 aaatcgtggc cccttcgacc tgcgctccgc gctctggcgc tacggtctgg ccgtcggctg 300 cggcgccatc ggagccctcg tactcggtgc tggtcttctc ttctctctcc ggtctgtgcg 360 ctcagtggtg cttcgagctg gagggcagca ggtgaccctc accactcatg ccccctttgg 420 cttgggggcc catttcacag ttcctttgaa gcaggtatct tgcatggccc accggggtga 480 agtccctgcc atgctacctc tgaaagtcaa aggccgacgc ttctatttcc tcttggacaa 540 aactggacac ttccctaaca caaaactctt tgacaatact gtgggtgcct accggagctt 600 gtgaagaaat gacctcaagt cactcacctc tccaagagga ggataaaaac tgaaccttgg 660 ggagccaggt gtgttggttc acgcctgttg taatcccagc actttgggag ggtgaggcag 720 gagcactgct cgagcccagg ctgggcaaca tagcgagacc ttgtctctat ttacaaaaaa 780 aaaaaaaaaa aaa 793 <210> SEQ ID NO 40 <211> LENGTH: 141 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 40 Met Ala Val Ala Ala Val Ser Arg Pro Pro Val Pro Val Gln Pro Leu 1 5 10 15 Asp Ala Glu Val Pro Asn Arg Gly Pro Phe Asp Leu Arg Ser Ala Leu 20 25 30 Trp Arg Tyr Gly Leu Ala Val Gly Cys Gly Ala Ile Gly Ala Leu Val 35 40 45 Leu Gly Ala Gly Leu Leu Phe Ser Leu Arg Ser Val Arg Ser Val Val 50 55 60 Leu Arg Ala Gly Gly Gln Gln Val Thr Leu Thr Thr His Ala Pro Phe 65 70 75 80 Gly Leu Gly Ala His Phe Thr Val Pro Leu Lys Gln Val Ser Cys Met 85 90 95 Ala His Arg Gly Glu Val Pro Ala Met Leu Pro Leu Lys Val Lys Gly 100 105 110 Arg Arg Phe Tyr Phe Leu Leu Asp Lys Thr Gly His Phe Pro Asn Thr 115 120 125 Lys Leu Phe Asp Asn Thr Val Gly Ala Tyr Arg Ser Leu 130 135 140 <210> SEQ ID NO 41 <211> LENGTH: 1970 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 41 atggcctgtc cgcgttaaac catcacaagc catggttgcg gaagggccac gcgtccccag 60 taggagaatg actccgattc gtgaccctca gcgccggtgc atgtcgatat atttattgag 120 tgtctactgt gtgccaggca ctatatctat gtgcatagaa aaaccctgga aggccgtaca 180 acaatatata tagagtgatc gtctctgctt gctgagctaa cagcaagttt atttctgatc 240 gtgaaagtag aagaagtctc acaaacagcc atttggaaaa aaagaagtgt gatgagtata 300 ttccaggtac aacctcctta ggcatgtctg tttttaacct aagcaacgcc attatgggca 360 gtgggatttt gggactcgcc tttgccctgg caaacactgg aatcctactt tttctggtac 420 ttttgacttc agtgacattg ctgtctatat attcaataaa cctcctattg atctgttcaa 480 aagaaacagg ctgcatggtg tatgaaaagc tgggggaaca agtctttggc accacaggga 540 agttcgtaat ctttggagcc acctctctac agaacactgg agcaatgctg agctacctct 600 tcatcgtaaa aaatgaacta ccctctgcca taaagtttct aatgggaaag gaagagacat 660 tttcagcctg gtacgtggat ggccgcgttc tggtggtgat agttaccttt ggcataattc 720 tccctctgtg tctcttgaag aacttagggt atcttggcta tactagtgga ttttccttga 780 gctgtatggt ttttttccta attgtggtta tttacaagaa atttcaaatt ccctgcattg 840 ttccagagct aaattcaaca ataagtgcta attcaacaaa tgctgacacg tgtacgccaa 900 aatatgttac cttcaattca aagaccgtgt atgctttacc caccattgca tttgcatttg 960 tttgccaccc gtcagtcctg ccaatttaca gtgagcttaa agaccgatca cagaaaaaaa 1020 tgcagatggt ttcaaacatc tcctttttcg ccatgtttgt tatgtacttc ttgactgcca 1080 tttttggcta cttgacattc tatgacaacg tgcagtccga cctccttcac aaatatcaga 1140 gtaaagatga cattctcatc ctgacagtgc ggctggctgt cattgttgct gtgatcctca 1200 cagtgccggt gttatttttc acggttcgtt catctttatt tgaactggct aagaaaacaa 1260 agtttaattt atgtcgtcat accgtggtta cctgcatact cttggttgtt atcaacttgt 1320 tggtgatctt cataccctcc atgaaggata tttttggagt cgtaggagtt acatctgcta 1380 acatgcttat tttcattctt ccttcatctc tttatttaaa aatcacagac caggatggag 1440 ataaaggaac tcaaagaatt tgggctgccc ttttcttggg cctgggggtg ttgtctcctt 1500 gtcagcattc ccttgtcatc tatgactggg cctgctcatc gagtagtgac gaaggccact 1560 gaacccgccg agaaaaagaa acatccctgt tgtctgctca gtcaagtccc cacacatcag 1620 caatctctca ccacttcttt tgcaagttta cagaagcaaa cagaaatgta caggatactt 1680 aaaatggaat aactttttgg ttgcaaaaca gagacatggt tctataatgc ttcatgtccc 1740 tccaagattt gagatcaatt tagggattgt gaattttttt tttcaaattt catacaatca 1800 tatttcccag tacttttcac aatcattttt tacccatcta actctatgtt ttgtggcttc 1860 ccggtctctt agaactttga aaacatgata tacaataatg tttatttatt atacatccag 1920 attctgaaat aattttccta ctgatggtca actctaaaaa aaaaaaaaaa 1970 <210> SEQ ID NO 42 <211> LENGTH: 412 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 42 Met Ser Val Phe Asn Leu Ser Asn Ala Ile Met Gly Ser Gly Ile Leu 1 5 10 15 Gly Leu Ala Phe Ala Leu Ala Asn Thr Gly Ile Leu Leu Phe Leu Val 20 25 30 Leu Leu Thr Ser Val Thr Leu Leu Ser Ile Tyr Ser Ile Asn Leu Leu 35 40 45 Leu Ile Cys Ser Lys Glu Thr Gly Cys Met Val Tyr Glu Lys Leu Gly 50 55 60 Glu Gln Val Phe Gly Thr Thr Gly Lys Phe Val Ile Phe Gly Ala Thr 65 70 75 80 Ser Leu Gln Asn Thr Gly Ala Met Leu Ser Tyr Leu Phe Ile Val Lys 85 90 95 Asn Glu Leu Pro Ser Ala Ile Lys Phe Leu Met Gly Lys Glu Glu Thr 100 105 110 Phe Ser Ala Trp Tyr Val Asp Gly Arg Val Leu Val Val Ile Val Thr 115 120 125 Phe Gly Ile Ile Leu Pro Leu Cys Leu Leu Lys Asn Leu Gly Tyr Leu 130 135 140 Gly Tyr Thr Ser Gly Phe Ser Leu Ser Cys Met Val Phe Phe Leu Ile 145 150 155 160 Val Val Ile Tyr Lys Lys Phe Gln Ile Pro Cys Ile Val Pro Glu Leu 165 170 175 Asn Ser Thr Ile Ser Ala Asn Ser Thr Asn Ala Asp Thr Cys Thr Pro 180 185 190 Lys Tyr Val Thr Phe Asn Ser Lys Thr Val Tyr Ala Leu Pro Thr Ile 195 200 205 Ala Phe Ala Phe Val Cys His Pro Ser Val Leu Pro Ile Tyr Ser Glu 210 215 220 Leu Lys Asp Arg Ser Gln Lys Lys Met Gln Met Val Ser Asn Ile Ser 225 230 235 240 Phe Phe Ala Met Phe Val Met Tyr Phe Leu Thr Ala Ile Phe Gly Tyr 245 250 255 Leu Thr Phe Tyr Asp Asn Val Gln Ser Asp Leu Leu His Lys Tyr Gln 260 265 270 Ser Lys Asp Asp Ile Leu Ile Leu Thr Val Arg Leu Ala Val Ile Val 275 280 285 Ala Val Ile Leu Thr Val Pro Val Leu Phe Phe Thr Val Arg Ser Ser 290 295 300 Leu Phe Glu Leu Ala Lys Lys Thr Lys Phe Asn Leu Cys Arg His Thr 305 310 315 320 Val Val Thr Cys Ile Leu Leu Val Val Ile Asn Leu Leu Val Ile Phe 325 330 335 Ile Pro Ser Met Lys Asp Ile Phe Gly Val Val Gly Val Thr Ser Ala 340 345 350 Asn Met Leu Ile Phe Ile Leu Pro Ser Ser Leu Tyr Leu Lys Ile Thr 355 360 365 Asp Gln Asp Gly Asp Lys Gly Thr Gln Arg Ile Trp Ala Ala Leu Phe 370 375 380 Leu Gly Leu Gly Val Leu Ser Pro Cys Gln His Ser Leu Val Ile Tyr 385 390 395 400 Asp Trp Ala Cys Ser Ser Ser Ser Asp Glu Gly His 405 410 <210> SEQ ID NO 43 <211> LENGTH: 812 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 43 gaacatggcg cgcggaaccg gcgcgcgcgc ctagctggcg ggaccgttag atcgaggcgg 60 atgcggcccg gaccccgtgg atatggagca gtcgccgccg ctggcgccgg agcccaccca 120 agggccaacc accgcaagga gctgaaggcg gcgggagccc gagtcgccgc cggcgtcggt 180 gccgtcaaag aagatggcca gggagacagc agcgtggtca gagtggtagg agctggccat 240 cggtgagagc tgctccatgc ctggctgctg ggttctagag cttgtggacc actggcttgc 300 ctcactgtgg ttggtggtgg cggtgacaga gtgtgcagca cgaccagagt ggcttttctg 360 gctttgccgc ccagctgctc catgccagga ggaggaggag acacctagag cctgcgacac 420 catggctcgc ctcgctgcag gttctaccca tgtaacagat gaggaaacca aggagcacag 480 ttatttacta actcgcacaa ggttcgaggc cgagctcaga cctgtggagc agaagctgag 540 tgcgctgcag tccccgctgg cccagaggcc cttcttcgag gtgccctcac ccctgggcgc 600 cgtggacctg tacgagtatg catgcgggga tgaggacctg gagccactgt gacgccaccc 660 atgagaacgc cgctgcgggg ccgctccaca cgtgccacgg ccaccactgg gacaccgccg 720 cttgtgtaaa aactgttgtc ttttgtggaa aatgagtgtg tttgcatgga atgataaatt 780 tttatttatt cacaaaaaaa aaaaaaaaaa aa 812 <210> SEQ ID NO 44 <211> LENGTH: 131 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 44 Met Pro Gly Cys Trp Val Leu Glu Leu Val Asp His Trp Leu Ala Ser 1 5 10 15 Leu Trp Leu Val Val Ala Val Thr Glu Cys Ala Ala Arg Pro Glu Trp 20 25 30 Leu Phe Trp Leu Cys Arg Pro Ala Ala Pro Cys Gln Glu Glu Glu Glu 35 40 45 Thr Pro Arg Ala Cys Asp Thr Met Ala Arg Leu Ala Ala Gly Ser Thr 50 55 60 His Val Thr Asp Glu Glu Thr Lys Glu His Ser Tyr Leu Leu Thr Arg 65 70 75 80 Thr Arg Phe Glu Ala Glu Leu Arg Pro Val Glu Gln Lys Leu Ser Ala 85 90 95 Leu Gln Ser Pro Leu Ala Gln Arg Pro Phe Phe Glu Val Pro Ser Pro 100 105 110 Leu Gly Ala Val Asp Leu Tyr Glu Tyr Ala Cys Gly Asp Glu Asp Leu 115 120 125 Glu Pro Leu 130 <210> SEQ ID NO 45 <211> LENGTH: 1533 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (360) <400> SEQUENCE: 45 ggattgaatt ctagaccagc ggccgcaggt ccgaagctca acggctctga gaagttgagc 60 tcccactggc tctaactgac ccaaagggat gtcagtggtg ttctggcttt ctggaaggcc 120 atcaaagtca ggcttcttcg ggcccccgag gcaggaaatg gggtctctcc atgggagaca 180 ggatgctgag gccgcggaaa gtcagcctcc tcacccccca ggtacgaggc caggaagggg 240 acgtcctcac caatgctggg tcccagctcc agcagcacgt cttctcggcc cagcttggtt 300 agcagctcga gcagtctgcc tacagaagcg ccaggggcct ccctgccagg cgtccagcan 360 cctgccagtt gggtccgctt gtgtctccag ttgccggatc tccaagttac tcaaagtcca 420 tctcctccgc cagcgcggtc aagtcggccg ccacctgtgt ccgctcgttc aagaacagag 480 acaggcggcg ccgcactcgc atgttgagag cagccagggg aagggaggat gtggaggaga 540 ccggggccgc agaccccgcg ccgggacctc ctgcagccat ggcgggcggt cctggagcct 600 cagcgcggtc gggtcgcatt gtctgccagc gcttcctctt tctcctgcgg cacccgcccc 660 gccccgccgg ctttcgcttt ccgagaagcg ccgccctgcc ctacaatctg gagccccgag 720 caaaagtgcg gaggcggggg tgcccacctc tacccttgag gtctcgaggc gggtgatgtg 780 gggggcgtaa gaagtaggaa tctgcctttt gagatctgga gaggtccacg gcaccgccct 840 cgaaggtctg gtgatggtgc tagtaggttg gcggcggagt gaggacaccc tccttcgggg 900 gttgtaggaa acgggccttg ctttttggga tctggtggag ccacagttct tccaccgaag 960 aatctgaggg gttcatacgg tcctgccctc caggatggcg aggaggggac aagtgggaag 1020 gcaccactct gccctccacc gtctcttggg gaacacacaa tcctgccagt agggtatggg 1080 aagaccctgc tgtgctcccc aagtgggagt ggaaacgaac actgccttct gagcgtgagc 1140 atgccgtggc cctgccctcg aaatggttgg ggatgtcatg acactaggtt ggggagcaca 1200 aggcaccctg tcctttggtg tctgtggaaa gcccagcact actctccagg gtctcaggtg 1260 aagacatggc cctgctattg ggagtccaag ggggcacgtg gccttgccct ttaggtttag 1320 ggacacagtc ctgacctggg gagccctggt tcattcattt actcattcga caagtactta 1380 ttgattatct actaagtgtc aagggtgtcg caggctcccc ggaaaaatgg aacctttttg 1440 ccttggtgga gaccccagcc tagcacggga aatgggcact aataaaatca tttccaattg 1500 ggtgtaaaac tggtaaaaaa aaaaaaaaaa aaa 1533 <210> SEQ ID NO 46 <211> LENGTH: 233 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (91) <400> SEQUENCE: 46 Met Ser Val Val Phe Trp Leu Ser Gly Arg Pro Ser Lys Ser Gly Phe 1 5 10 15 Phe Gly Pro Pro Arg Gln Glu Met Gly Ser Leu His Gly Arg Gln Asp 20 25 30 Ala Glu Ala Ala Glu Ser Gln Pro Pro His Pro Pro Gly Thr Arg Pro 35 40 45 Gly Arg Gly Arg Pro His Gln Cys Trp Val Pro Ala Pro Ala Ala Arg 50 55 60 Leu Leu Gly Pro Ala Trp Leu Ala Ala Arg Ala Val Cys Leu Gln Lys 65 70 75 80 Arg Gln Gly Pro Pro Cys Gln Ala Ser Ser Xaa Leu Pro Val Gly Ser 85 90 95 Ala Cys Val Ser Ser Cys Arg Ile Ser Lys Leu Leu Lys Val His Leu 100 105 110 Leu Arg Gln Arg Gly Gln Val Gly Arg His Leu Cys Pro Leu Val Gln 115 120 125 Glu Gln Arg Gln Ala Ala Pro His Ser His Val Glu Ser Ser Gln Gly 130 135 140 Lys Gly Gly Cys Gly Gly Asp Arg Gly Arg Arg Pro Arg Ala Gly Thr 145 150 155 160 Ser Cys Ser His Gly Gly Arg Ser Trp Ser Leu Ser Ala Val Gly Ser 165 170 175 His Cys Leu Pro Ala Leu Pro Leu Ser Pro Ala Ala Pro Ala Pro Pro 180 185 190 Arg Arg Leu Ser Leu Ser Glu Lys Arg Arg Pro Ala Leu Gln Ser Gly 195 200 205 Ala Pro Ser Lys Ser Ala Glu Ala Gly Val Pro Thr Ser Thr Leu Glu 210 215 220 Val Ser Arg Arg Val Met Trp Gly Ala 225 230 <210> SEQ ID NO 47 <211> LENGTH: 3023 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 47 tcacattgcc aaaagacggc aatatggtgg aaaataacat atagacaaac gcacaccggc 60 cttattccaa gcggcttcgg ccagtaacgt tagaattgcc gagaagtcat gataatttcg 120 tttgttcttc cagatttagg catatactta tttaatcaat aatgtgttaa cagctgacac 180 ctgtggttgc tgtgacaggc actatttgaa gtgctttatc atggattaac tcttaatcct 240 cagctaccgt ataaagtagg acataacccc atttcacatg cactacactg agacttgcct 300 cctctccccc cacattgaag atgttctttt ttcataacta tatactattc cattgcatga 360 atattctgta atttatttaa tcccctatgg attgataatt aggttcatta tagatagaag 420 tgtaattaac attcctgtac atgtattttg ctacttgtgt gggtatttct gtaggatgaa 480 taactagaaa tttattggat caggtttcac atttgcagtt ttgaaaacta ctaccaaaaa 540 gatttcacca atttacaact ccatcattag taagaatgcc tgtttgccta tagtctgcca 600 accctgaatc cttaaaaatt tttgccaatc tggtaggcaa aatttctttc ttttctttga 660 atattaatga ggaggaacat cttttcatgt ttcttggcca tttgcatttc ctattatgaa 720 ttgcttttgc ccattttcct ttttttaatt atgaaagtct aatgactacc ttctcattgt 780 ataaaaaaca cagttctttg aatagagaga cccttttctc caatgctacc aatcacattc 840 cacttaccac agtttaacat acatcctcta gtcacctttc cgtacgaata tacatacaca 900 taaaaacact ttttacataa ataggatctc atattctgta gctttttaaa attttggtct 960 caaaaaaaga taacaggtct ttaaatttct ttaatggttg actatgatta aatactatga 1020 aaatgccatt atttattccc ttaatttttt tccctctcgc tattacattg ccaaagttaa 1080 catcctattc agatgtcttt gtgcatgtgt gtgaatattt ctttagtctg gagtccagta 1140 aggtggattt ttggatcaaa gggtttgttc tctgtccacc ttcagtcttc ccaaaggcct 1200 tcataactgt attttcacca agtgtatgga gaatgttcat ttccccatat aaccatacct 1260 acacttgata gtttttatct gttgggcgaa aaagaacctt ttcttatttt gcatttccct 1320 gattataaaa aaaaatggtg agattggggt tattttcatg tttattggcc atttatagtt 1380 tactgtggat tgtttgtatc ccttacctgc tttctattgg gttatgtgtg gatatattgt 1440 ttttatttgt tcagcatctc cttccccatc ttctggtaac acaaccttta tttatttgtg 1500 gggaacctat tccctgtggc ttaggtgagc atgtgaccag gcctggcctc ctgagtccca 1560 cagcttccta gccacagtga taaaagaatg ggtatataac ttaagccagg ctaaggaaag 1620 cccttaacag aacttctgct ggaactactg gaaagaaggc tttatggaga tcccaggaac 1680 caaggaccat gtaagcctga atttgtgcca tgtggagaga gtctgtctga ggagaaactc 1740 ggatgctagc agaaatggaa agagaactaa gttctgatgt catttttctg gaggccctag 1800 atccagctgt gcctaaagcc tgccctacct ccggacttta aagttttgtg agccaataaa 1860 gtccctttct tgtttaagat aattgaattg agtttctgtt ctgattaata taggttatgt 1920 gtattttctt attgatttgt agaaaacctt gtaattttaa attctagact ttatgcccta 1980 tataagttac taaactctgt ctcaataaaa aaaaaggaaa acccacagcc aacattatca 2040 ctagtggtaa cagggaaaat gtcccctttg acccccaccc caagtacaga acatgcaagg 2100 acgcctgttc tcactgcatg tcttctgtgt tgtactgaag ctcctagctg gtgcagtgag 2160 gcaagacaaa gaaaggaaat ataggtgcac tgggaaggaa gaagaaacac tgcctttatt 2220 ctttaggtga catgattgtg tgcttttaaa ataataaagg aatcaacaga aaagttgctt 2280 aacctaatga atgagtttat caaagtcaca agatacaagg tcagtataca aaaatcagtt 2340 ggatttctac atggtagaaa caactgtaca tggaaaaatg tttaatagtg taagatatgt 2400 acattggaaa ctatgaaaga gtgtaaaaaa taaagaagtg aaataaatgg agaagatacc 2460 accttgatgg atggaagcct taaggtaaag atgctcattc tccccacact gacctgtaca 2520 ttccccacag gcctaatcaa aacccccaca ggcttctgtg tagaaattga catgctgatc 2580 ctgaaattta tatgaaaatg caaagagtct ggaataacca aaataatttt gtaaaagaac 2640 aaagaagact tctactacct ggttataaga cttctctgaa gcacagaagt caaggcagtg 2700 tggtggtggc ataagtaatg taaatcatcc aggtgtggtg gctcaggcca gtcatccagc 2760 actttgggag gctgaggcag gagaatcgct agagcccagg agttggaaac cagcctgggc 2820 agcatagcaa gactcatctc tacaaaaaat acgaaacaat tagctgggtg tctgtagcac 2880 atgcctgtag tcccagctgc gcgggaggct gagctgggaa gatcacttta gcctgggaag 2940 tcaggggagc tgtgatcaca ccactgcact ccagcctggg caacagagca agaccccatc 3000 tcaaaaacaa aaaaaaaaaa aaa 3023 <210> SEQ ID NO 48 <211> LENGTH: 83 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 48 Met Lys Met Pro Leu Phe Ile Pro Leu Ile Phe Phe Pro Leu Ala Ile 1 5 10 15 Thr Leu Pro Lys Leu Thr Ser Tyr Ser Asp Val Phe Val His Val Cys 20 25 30 Glu Tyr Phe Phe Ser Leu Glu Ser Ser Lys Val Asp Phe Trp Ile Lys 35 40 45 Gly Phe Val Leu Cys Pro Pro Ser Val Phe Pro Lys Ala Phe Ile Thr 50 55 60 Val Phe Ser Pro Ser Val Trp Arg Met Phe Ile Ser Pro Tyr Asn His 65 70 75 80 Thr Tyr Thr <210> SEQ ID NO 49 <211> LENGTH: 1049 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 49 gtaactatct ccatgtttgt ccttttctac ctcgtttttt caccactccc aaacataacc 60 tcccaatctt ttttgttagt ccggccgtca atttgtatag taccaatttc tgtaaattct 120 ctcaattcat tgaagatcgt agggttaaac ttttttgtgt gtgatttaaa cttacaaaca 180 agtgaagaag ctatcgttta tttcagacga ggctgtagtt taaataccaa aagagggaaa 240 ataaaaaaga acctttgtaa aatatatctg aacctaatgg tttgtacact ggagaatcgt 300 tctagatagt taccaattaa atataactcc gccagtgtaa gggtgtgagg tgcagttgtc 360 caggagacga ttttgtatag tatttttctt gtacattact tccagtaaat atttgaaaat 420 atattgaagt aaacttgatt ttttttttgt cacaagaaaa tattaagagt tattgttgca 480 gttctgatga gctgcaggtt ttttgaactc acttctggag gtgcagagcc acaaacgcac 540 tttcggggcc tagttttgct cgaatatgaa tttagatagg tatcaagctg taactaagac 600 aatatttgat aaatgttgga tgacatttaa tttaatggag catgtactta tttgcatttg 660 ctggcagttc aggcatagtt aaagtgagag ttctccgata tttcataata agtgggtctg 720 ccaaaaccca tgtattaaat aaattgtcca agtgaaactc gactaacttt ggcctttgtg 780 tatttcctga aggtaatatt gttaactgtt aataaatact tctgacacta catttaaatg 840 tttgcagatt ctgcaaacta attgctcatt gtaatgttga aataatttgg atatttcaca 900 ttgaaatgaa aagcctttct ctggagcatt ttagatttgc attttaaatg catgaaatgt 960 aattgattta tttgtaaaat tttaaatggg gttaataaac tcagaaaaaa aaaaaaaaaa 1020 aaaaaaaaaa aaaaaaaaaa aaaaaaaaa 1049 <210> SEQ ID NO 50 <211> LENGTH: 98 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 50 Met Phe Val Leu Phe Tyr Leu Val Phe Ser Pro Leu Pro Asn Ile Thr 1 5 10 15 Ser Gln Ser Phe Leu Leu Val Arg Pro Ser Ile Cys Ile Val Pro Ile 20 25 30 Ser Val Asn Ser Leu Asn Ser Leu Lys Ile Val Gly Leu Asn Phe Phe 35 40 45 Val Cys Asp Leu Asn Leu Gln Thr Ser Glu Glu Ala Ile Val Tyr Phe 50 55 60 Arg Arg Gly Cys Ser Leu Asn Thr Lys Arg Gly Lys Ile Lys Lys Asn 65 70 75 80 Leu Cys Lys Ile Tyr Leu Asn Leu Met Val Cys Thr Leu Glu Asn Arg 85 90 95 Ser Arg <210> SEQ ID NO 51 <211> LENGTH: 1707 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 51 cacacagctc ccggatgaag ataacagttg gtagaccaaa aggtgacctc gcttagtata 60 ttgaaaacac acaccacaca tcacacacag aactgaatca taccacgtgc tgcctatggg 120 acttcagtta ctgtttcctg agttactgtt tatccgctgg caatggtgtg atttgtctgg 180 atcagatccg tgctattccc caacccacct ccagataatg tgagaaaata gccatgtcag 240 tatgtaggaa ctctgatggt gctcagattt gtgtgttcaa tcaatgggct taaatcagca 300 aaatattatg cctaaagtaa atctgttctt aacaagggct ctaccactgc attttcacat 360 gtaccttcag ggggttatct tttttttttt cccctcctat tttaatcagc aaaatccata 420 ccaaaacaac gacaacaacg ccctcttaag ggaccaccct ttggtcaatc ataacatgct 480 gtttaaagca gctgtttaca ggatgtgtag tggtatgccc ttgtcatata ctcttagcat 540 atcttttttt cctttggctt tgcatggctt tcttcaggta ctgtctcggt atcattctgc 600 taatcattgt tacagaatgg tgacttcatt tgtgctaaca gtacaacagc agatttgggt 660 caggcttaat ctagtgttaa cttttttttc tggtgctttt ttggattgat gactgtctca 720 ctttgactat acccatgttt tgcatgcaat gactcatgca tggttttctt aactagctaa 780 tattaacaat ttattccata taaaaatgga attttgcaac atcctttaat aaggtgaggg 840 aagcatgaac ctcagacttc tggcactatt acatagtaag cacatgaagt agtttgataa 900 taaatagcag ttctagtact tcacatttca cccgtgtgtg caatgccttt ttctgggggg 960 tggggggtga gggaaaacct ggtagtgaat gtgtagttgg ggaataaaga aaagcactaa 1020 atcctgccct ttttgtgtgg tttccttttg atacaactag gttattcata atgtatacct 1080 agaaaagtga aattgaaaat accaaaagat gtatcatttt tatttgaatc catcatgcag 1140 tgtacatttc agataatttc cttcagtctc cagataggag tgtatccaaa catctaattt 1200 tatgtgcact gtgtatctta tatgaatgtt ttattttata taccacatgc aaaaatgtcc 1260 atatgcacta tttaaatgtt ttaaataata tattccttct ttataatgct aaatctatat 1320 gagtaccata tttttataag tcagtggtct gactggtttc attttagaat taacagctgc 1380 ttcaatatgt tattcaatgt taatgtttgg ctgtgagtag aatatgtaaa agtggcatgg 1440 cagcacttat gctctgtgac agtattgtgt gtcatagttg agcagtagct ggtagaatta 1500 ggcagttggt gatagtttta ctttggtaca aataaaaact gtatatctat atacaaataa 1560 tatatagata tatatgtcca ccagtataat ggcattgctg tgtctggcac ttcattgtac 1620 ggacttttat aataaaagaa cttgaaagtt tttaaaaaaa aaaaaaaaaa aaaaaaaaaa 1680 aaaaaaaaaa aaaaaaaaaa aaaaaaa 1707 <210> SEQ ID NO 52 <211> LENGTH: 141 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 52 Met Gly Leu Asn Gln Gln Asn Ile Met Pro Lys Val Asn Leu Phe Leu 1 5 10 15 Thr Arg Ala Leu Pro Leu His Phe His Met Tyr Leu Gln Gly Val Ile 20 25 30 Phe Phe Phe Phe Pro Ser Tyr Phe Asn Gln Gln Asn Pro Tyr Gln Asn 35 40 45 Asn Asp Asn Asn Ala Leu Leu Arg Asp His Pro Leu Val Asn His Asn 50 55 60 Met Leu Phe Lys Ala Ala Val Tyr Arg Met Cys Ser Gly Met Pro Leu 65 70 75 80 Ser Tyr Thr Leu Ser Ile Ser Phe Phe Pro Leu Ala Leu His Gly Phe 85 90 95 Leu Gln Val Leu Ser Arg Tyr His Ser Ala Asn His Cys Tyr Arg Met 100 105 110 Val Thr Ser Phe Val Leu Thr Val Gln Gln Gln Ile Trp Val Arg Leu 115 120 125 Asn Leu Val Leu Thr Phe Phe Ser Gly Ala Phe Leu Asp 130 135 140 <210> SEQ ID NO 53 <211> LENGTH: 1922 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 53 aaagcaccag gaactggttg accacctttc ccagcatgtc tcttaggggc ctgacctcag 60 gatttcagac tggattcact gtgacagaac taagggaata aatacatttt atgtccacgt 120 tcccactctg gtgtaccatc tgtccacaga ggggagagaa caagcaagag gttggggtgt 180 gccatccagt gtcccctgga gcagaccttg gcctctggtc ttcagtgccc ggtcctcctg 240 tctgttgtct ggcctggtga ggaagccctg acttgtaact ctcaaagcct aacttcaggg 300 gttgccctgc cagtgccctc tccgggagct ttgggtccct ggttataagc tttcagttct 360 cagtgtctgc tgtcaccagt aaccaagtgc tgaaaatgat ctgtaccact ttgctgacaa 420 gggcggctgg gccagggtgc ccccgcccag cttcctctac tctccctgtg gcctggggct 480 acacttgggt taaaactccc cattatggag ccaactgatt ctcccacttg gccccagggc 540 atgatttaag caaacttaaa actcaatgct ttattgatag tttaaataat taacattacg 600 taaagaaaaa tctaaatgta aacagttttt gcaaacgagt atccattaag ggacttccaa 660 gtacctaacc cctattaaac aatttatgta aaccactctt ccttaaagaa aatcgaatgc 720 ccagctcctt cccaatcctc caagctctga agtagggaag aggtgcagct aggagcagat 780 ggggcagtgt gtgtgttgga ggtggaggag tgggggaaat caaatcagct cacctgtgtg 840 gttatttatc agtgaaactt aataaactgg tactgggaaa gaaaaggagg ctagtgattg 900 acagcatccc gggctgctga gaggaccagc atgatgagct gtcttggagt tggcaattag 960 gagctcgtga gcgacctttg ccagaacagt tccatgggac gacctggctg gaggcctaat 1020 tgcaacagat ttatgatctt gcttggccag atatcctggg aggcagaaac gaggactgtt 1080 ctgaacatat gcatcaggac gcataatggg gctttgttcg ggcctgggca gacatggagg 1140 gcaatgcctg agctctcttc cagtttatct ccacgtcctc caagctcaaa tctggcagcc 1200 ctggagtggt ttgaagttga aactccacag agcagtggac ttaatgctcc aaagatgcgt 1260 tgacattcag ccattgtccc tggcccccaa gtgtccgtgg gagttgctga gttttcatgg 1320 agatgatcca cgtccctggg tgtcgcctgc ttcctctcac agtgtgaaaa ccacacagct 1380 actgttacta gagatcatcc tggaatttct gggacagccc ttgtttaaag cactctgtgt 1440 tccagattga tcagacacgt ctctctccac cccttcacaa aactccacta aaaagagtga 1500 gaaattttaa agggtgcaca ttcacaacta cagagagaat gaaaaagatg tcagtgaaga 1560 agagattatg cattctgggg caatggaaag cggatagagg ctgggcacag tggctcactc 1620 ctgtattccc agcactttgg gagcccaagg caggcggatc acctgaggtc agaagttcaa 1680 gaccagcctg gccaacgtgg tgaaacccca tctctacaaa aatacaaaaa ttagctgggc 1740 atggtggtgg gtacctgtag tcccagctac tcaggaggct gaggctactc gggaatcaca 1800 tgaacccaag aggcggaggt tgcagtgagc aggtatcacg ccaatgcacc ccagcctggg 1860 caacaaagcg agaatctgtc aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 1920 aa 1922 <210> SEQ ID NO 54 <211> LENGTH: 114 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 54 Met Gly Leu Cys Ser Gly Leu Gly Arg His Gly Gly Gln Cys Leu Ser 1 5 10 15 Ser Leu Pro Val Tyr Leu His Val Leu Gln Ala Gln Ile Trp Gln Pro 20 25 30 Trp Ser Gly Leu Lys Leu Lys Leu His Arg Ala Val Asp Leu Met Leu 35 40 45 Gln Arg Cys Val Asp Ile Gln Pro Leu Ser Leu Ala Pro Lys Cys Pro 50 55 60 Trp Glu Leu Leu Ser Phe His Gly Asp Asp Pro Arg Pro Trp Val Ser 65 70 75 80 Pro Ala Ser Ser His Ser Val Lys Thr Thr Gln Leu Leu Leu Leu Glu 85 90 95 Ile Ile Leu Glu Phe Leu Gly Gln Pro Leu Phe Lys Ala Leu Cys Val 100 105 110 Pro Asp <210> SEQ ID NO 55 <211> LENGTH: 589 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 55 tttttccaca ctcagctttc ccctagcatg gacaagattt tcagccattt ttgccacata 60 tacattttta aggaaaaaag atttttctct gtaagaaagt tctggttatg ctgttttaaa 120 ggtgacttgt caggagttga gacttccctg ccggattcta ttttgaaagt aaatggtctt 180 ccctccttgt tccgattctg cgttcccatc gtcagacaac tttggagtat tagaaaccac 240 tgtatatatg tggaaagcca ggtcagccag actgttagat tggtgtgcac tcacctgaga 300 gatctggcag gttggatata tttatgtgta tttctccaca gtgcttgctt tgccctgttg 360 gtaaggattt taaataacca tgctcaaaag agctgttcta atctgcgttt tgcatgttaa 420 gtgttaatat caaacattct taacgtgctc gaggaattgc ttttaacatt ctactttgcc 480 agtttcttca ttagattaat tgacatgtat tatttaaatg accagtgatg ctttgtgcaa 540 ttatgaatgt tgaagattaa agtacatagt tactaaaaaa aaaaaaaaa 589 <210> SEQ ID NO 56 <211> LENGTH: 130 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 56 Met Asp Lys Ile Phe Ser His Phe Cys His Ile Tyr Ile Phe Lys Glu 1 5 10 15 Lys Arg Phe Phe Ser Val Arg Lys Phe Trp Leu Cys Cys Phe Lys Gly 20 25 30 Asp Leu Ser Gly Val Glu Thr Ser Leu Pro Asp Ser Ile Leu Lys Val 35 40 45 Asn Gly Leu Pro Ser Leu Phe Arg Phe Cys Val Pro Ile Val Arg Gln 50 55 60 Leu Trp Ser Ile Arg Asn His Cys Ile Tyr Val Glu Ser Gln Val Ser 65 70 75 80 Gln Thr Val Arg Leu Val Cys Thr His Leu Arg Asp Leu Ala Gly Trp 85 90 95 Ile Tyr Leu Cys Val Phe Leu His Ser Ala Cys Phe Ala Leu Leu Val 100 105 110 Arg Ile Leu Asn Asn His Ala Gln Lys Ser Cys Ser Asn Leu Arg Phe 115 120 125 Ala Cys 130 <210> SEQ ID NO 57 <211> LENGTH: 1363 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 57 gtagtggact tgatcttcct taacacagaa gtgtcactgt cacaagcctt ggaggatgtt 60 agcaggggag gttctccttt tgctattgtc atcacccagc aacaccagat tcaccgctcc 120 tgcacagtca acatcatgtt tggaaccccg caagagcatc gcaacatgcc ccaagcagat 180 gccatggtgc tggtggccag aaattatgag cgttacaaga atgagtgccg ggagaaggaa 240 cgtgaggaga ttgccagaca ggcagccaag atggccgatg aagccatcct gcaggaaaga 300 gagagaggag gccctgagga gggagtgcgt gggggccacc ctccagccat ccagagcctc 360 atcaacctgc tggcagacaa caggtacctc actgctgaag agactgacaa gatcatcaac 420 tacctgcgag agggaaggag cggctgatga ggagcagcac cgactctctg cctggggagc 480 tacgtggcag ggccgaggcc cgatttcccg ccaaccactc ggggcgacct cgggtgcctc 540 gctgaagaca cagccaagct cccaaccgct ccagagcggc caagtgctcc cctctgctac 600 acccactcca tctgcacccc ccacctccca gcaagagctt caggccaaaa tcctcagcct 660 cttcaatagt ggcaccgtga cggccaatag cagctctgca tccccctcgg ttgctgccgg 720 aaacacccca aaccagaatt tttccacagc agcaaacagc cagcctcaac aaagatcaca 780 ggcttctggc aatcagcctc caagcatttt gggacaggga ggatctgctc agaacatggg 840 ccccagacct ggggctcctt cccaagggct ttttggccag ccttccagtc gcctggcacc 900 tgctagcaac atgactagcc agaggcctgt gtcttccaca ggtatcaact ttgacaatcc 960 aagtgtacag aaggctctgg ataccctgat ccagagtggc cctgctctct cccacctggt 1020 tagccagacc acagcacaga tggggcagcc acaggccccc atgggatctt accagaggca 1080 ttactgagag ctaaatcttt caactctccc cagtcccctc atcccctggc ctcctcccac 1140 ttacttgttc taaatagagc tgtttggagg atgttctctg cgctcccagg ccggcatcga 1200 gtgtcatcaa tttctaccac ctgctctctc ttctgcccaa ggctgtgttg cttattcctt 1260 acaaagttta tactgcattt ggggctgtat ctttttttgt tttttgtttt gtagaaaata 1320 aaaatctccg ggggcaaaaa aaaaaaaaaa aaaaaaaaaa aaa 1363 <210> SEQ ID NO 58 <211> LENGTH: 343 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 58 Met Leu Ala Gly Glu Val Leu Leu Leu Leu Leu Ser Ser Pro Ser Asn 1 5 10 15 Thr Arg Phe Thr Ala Pro Ala Gln Ser Thr Ser Cys Leu Glu Pro Arg 20 25 30 Lys Ser Ile Ala Thr Cys Pro Lys Gln Met Pro Trp Cys Trp Trp Pro 35 40 45 Glu Ile Met Ser Val Thr Arg Met Ser Ala Gly Arg Arg Asn Val Arg 50 55 60 Arg Leu Pro Asp Arg Gln Pro Arg Trp Pro Met Lys Pro Ser Cys Arg 65 70 75 80 Lys Glu Arg Glu Glu Ala Leu Arg Arg Glu Cys Val Gly Ala Thr Leu 85 90 95 Gln Pro Ser Arg Ala Ser Ser Thr Cys Trp Gln Thr Thr Gly Thr Ser 100 105 110 Leu Leu Lys Arg Leu Thr Arg Ser Ser Thr Thr Cys Glu Arg Glu Gly 115 120 125 Ala Ala Asp Glu Glu Gln His Arg Leu Ser Ala Trp Gly Ala Thr Trp 130 135 140 Gln Gly Arg Gly Pro Ile Ser Arg Gln Pro Leu Gly Ala Thr Ser Gly 145 150 155 160 Ala Ser Leu Lys Thr Gln Pro Ser Ser Gln Pro Leu Gln Ser Gly Gln 165 170 175 Val Leu Pro Ser Ala Thr Pro Thr Pro Ser Ala Pro Pro Thr Ser Gln 180 185 190 Gln Glu Leu Gln Ala Lys Ile Leu Ser Leu Phe Asn Ser Gly Thr Val 195 200 205 Thr Ala Asn Ser Ser Ser Ala Ser Pro Ser Val Ala Ala Gly Asn Thr 210 215 220 Pro Asn Gln Asn Phe Ser Thr Ala Ala Asn Ser Gln Pro Gln Gln Arg 225 230 235 240 Ser Gln Ala Ser Gly Asn Gln Pro Pro Ser Ile Leu Gly Gln Gly Gly 245 250 255 Ser Ala Gln Asn Met Gly Pro Arg Pro Gly Ala Pro Ser Gln Gly Leu 260 265 270 Phe Gly Gln Pro Ser Ser Arg Leu Ala Pro Ala Ser Asn Met Thr Ser 275 280 285 Gln Arg Pro Val Ser Ser Thr Gly Ile Asn Phe Asp Asn Pro Ser Val 290 295 300 Gln Lys Ala Leu Asp Thr Leu Ile Gln Ser Gly Pro Ala Leu Ser His 305 310 315 320 Leu Val Ser Gln Thr Thr Ala Gln Met Gly Gln Pro Gln Ala Pro Met 325 330 335 Gly Ser Tyr Gln Arg His Tyr 340 <210> SEQ ID NO 59 <211> LENGTH: 1613 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 59 cctcgctaca caagaaaagt tgtgtcctgg tttaagcttt gactgaaact cattcacatc 60 cgtgtgttaa tttgcatttt caggcctctt ctctctgaat ctctcctaga gaagaaaatt 120 atggaatagt tggttgcttt ctgtttgggg tcaggagaat tagggagaga tttctctttg 180 tttccaatgg atcctgaagg tgagctgcca tcacctcatc tctaggaggt gctgtaggga 240 gaaaaactgg aggtagcagg gtatttctct ctcttttctc ccctccgtct agccttaatt 300 aatagtttca tcttttgggt catcgaaaaa gtcagctctg attcatccat atccaataaa 360 ttgcagggtc acatggatcg ggtcttccga gccacctgcc ttctttttct caagttccct 420 ggtggcgcct cttcaggtcc tcacatctct tctgtcccgt cacagaggaa cacctcagac 480 ccatcctctc taccttggca tatcaccccc tggtcccttg atgcttcttc cttctggtcc 540 tcggagtctt ttctgagctc cagcgtcacc ggcgttggtg gcctttccac cctcccctct 600 cgcatgtgcc ttttccagtc cattgggact actccctgct cccccgtcac acacgttccc 660 taggccagtt ccttttcacc tggctgtagt cctcatgacc agctaaaagt gcgcctgccc 720 cagatatttg tgatttccct ctcttcagag aaagcaggga gcccctggca tccctatctg 780 tgacaggtgc cacacccgcc ttacaatgca ggtctgtgtg cccttgttgt atccctaact 840 gctctcaaat cccttagtga cggcctcatt tctctgcctt tgtgtagcat ttaaacagtt 900 taaatggctg ggcacgtggc tcacatctct aatcccagca ctttggaagg ccaaggcggg 960 acgatcactg gagtctcggg gagttcgaga ccagcctggc caacatggtg aaaccccttt 1020 ctactaaaaa tacagaaatc ggcgggctgg ttggtgcgtt cctgtaatcc cggctactgg 1080 gggggctaag gagggagaat tgtttggacc cgggaggttg cagtgagcag agtatgcgtc 1140 attgcactcc agattgggga acaagagcga gactctgtct caaaataagt aagttgataa 1200 aagtgaacag tttaaatgga tgaacctttg accctgcagt aaattccaga catgtaggag 1260 aaacagccag gtgtagaggg aaggcagtgg ggttctgagt caggcagacc taagtttggc 1320 atctggctcc tgtgctggtg gctgagttcc ttaacctttg tgtgttctta cagctctgtg 1380 ggtctcaatt gttccaccta taaaacaggg atgacactgt gacctttcag ggttgtggag 1440 tagttgtgtg atgttccttg tttaggccag gcccagtggc tcacgcctgt aatcccaata 1500 ctttgggaag ccaaggtgag tggattgctt gagccccgta gtttgagacc agcctacaca 1560 acatggcaag accccatctc cgcaaaaaaa aaaaaaaaaa aaaaaaaaaa aaa 1613 <210> SEQ ID NO 60 <211> LENGTH: 96 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 60 Met Asp Arg Val Phe Arg Ala Thr Cys Leu Leu Phe Leu Lys Phe Pro 1 5 10 15 Gly Gly Ala Ser Ser Gly Pro His Ile Ser Ser Val Pro Ser Gln Arg 20 25 30 Asn Thr Ser Asp Pro Ser Ser Leu Pro Trp His Ile Thr Pro Trp Ser 35 40 45 Leu Asp Ala Ser Ser Phe Trp Ser Ser Glu Ser Phe Leu Ser Ser Ser 50 55 60 Val Thr Gly Val Gly Gly Leu Ser Thr Leu Pro Ser Arg Met Cys Leu 65 70 75 80 Phe Gln Ser Ile Gly Thr Thr Pro Cys Ser Pro Val Thr His Val Pro 85 90 95 <210> SEQ ID NO 61 <211> LENGTH: 1700 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 61 aagctgtgcg aggagttcct ggcgcacgcc cgcggccggc tggagaagga gctgagaaac 60 ctggaggccg agctggggcc ctcacctccg gctcccgacg tgttagagtt caccgaccat 120 ggaggcagtg gcttcgtggg cggcctctgc caggtggcgg cggcctacca ggagctgttt 180 gcggcccagg gcccagcagg tgccgagaag ctggcggcct tcgcccggca gctgggcagc 240 cgctattttg cgctggtgga gcggcggctg gcgcaggagc agggtggtgg tgacaactca 300 ctgctggtgc gggcgctgga ccgcttccac cggcgcttgc gggctcccgg ggccctgctg 360 gccgctgccg ggctcgcaga cgctgccacg gagatcgtgg aacgagtggc ccgcgagcgc 420 ctgggccacc acctgcaggg tctccgggcg gccttcctgg gctgcctgac agacgtccgc 480 caggcgctgg cagcacctcg cgtggctggg aaggagggcc ctggcctggc cgagttgctg 540 gccaatgtgg ccagctccat cctgagccac attaaggcct ctctggcagc agtgcacctt 600 ttcaccgcca aagaggtgtc cttctccaac aagccctact tccggggtga gttctgcagt 660 cagggtgtcc gtgagggcct catcgtgggc ttcgtccact ctatgttcca gacggctcag 720 agcttctgcg acagccctgg ggagaaaggg ggtgccacac cacctgccct gctcctgctg 780 ctctcccgcc tctgcctgga ctacgagacg gccaccatct cctacatcct cactctcact 840 gatgaacagt ttctggtgca ggatcagttc ccagtgacgc ccgtgagcac gctgtgtgca 900 gaggccaggg aaacggcgcg gcggctgctg acccatacgt gaagtgcagg gcctggtcat 960 atcacagatg ctgcgcaaga gcgtggagac tcgcgactgg ctcagcactc tggagccccg 1020 gaatgtgcgg gctgtcatga agcgggtggt ggaggatacc accgccatcg acgtgcaggt 1080 ggggctcctg tacgaagagg gtgttcgcaa ggcccagagc agcgactcca gcaagaggac 1140 tttctccgtg tacagcagct ctcggcagca gggccgctac gcccccagct atacccccag 1200 tgccccgatg gacaccaacc tcttgagcaa tatccagaag ctattctctg aacgtattga 1260 tgtgttcagc cctgtggagt tcaacaaggt gtcggtgctg accggcatca tcaagatcag 1320 cctgaagacg ctgctggagt gtgtgcggct gcgcaccttt gggcgcttcg ggctgcagca 1380 ggtgcaagtg gactgccact ttctgcagct ctacctgtgg cggttttgtg gccgacgaag 1440 aactcgtgca cttgctgctg gacgaagtgg tggcctctgc tgccctgcgc tgcccagacc 1500 ctgtgcccat ggagcccagt gtggttgagg tcatctgcga gcgcggctag gcgcagccgc 1560 tgccatgcac cggtctgtcc ctgcacccca tggcacccag gatctggtct cggtggtcct 1620 tccccgcagg caggtgtcag gaccggccta ataaacatgt gtggcctccc caaaaaaaaa 1680 aaaaaaaaaa aaaaaaaaaa 1700 <210> SEQ ID NO 62 <211> LENGTH: 116 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 62 Met Glu Ala Val Ala Ser Trp Ala Ala Ser Ala Arg Trp Arg Arg Pro 1 5 10 15 Thr Arg Ser Cys Leu Arg Pro Arg Ala Gln Gln Val Pro Arg Ser Trp 20 25 30 Arg Pro Ser Pro Gly Ser Trp Ala Ala Ala Ile Leu Arg Trp Trp Ser 35 40 45 Gly Gly Trp Arg Arg Ser Arg Val Val Val Thr Thr His Cys Trp Cys 50 55 60 Gly Arg Trp Thr Ala Ser Thr Gly Ala Cys Gly Leu Pro Gly Pro Cys 65 70 75 80 Trp Pro Leu Pro Gly Ser Gln Thr Leu Pro Arg Arg Ser Trp Asn Glu 85 90 95 Trp Pro Ala Ser Ala Trp Ala Thr Thr Cys Arg Val Ser Gly Arg Pro 100 105 110 Ser Trp Ala Ala 115 <210> SEQ ID NO 63 <211> LENGTH: 1616 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (869) <400> SEQUENCE: 63 tcttaatata tgcacatatg tatatgtaac acataaataa ttacatacat aatacaggaa 60 gacacagaaa taattacata catgatacag gaagacacag aaaaagagaa actggtctga 120 taccagaagt atcaactcag gaacaatttt ctactagctg agcctcagaa gcagcaactt 180 ttccaaagtg aagtgatgaa tggaggcgcc agccctcctc ctcaggttaa gaaaggcaaa 240 gagccctgct tttggctgta aaaagccagg ttccctaatc aggtgaaggc ctgaggcagg 300 gactccttag ggcagtgtaa ctagtagcca aggcacaggc tccaaaggga ggttgcctgg 360 gctcaagccc ggctctgcca cttcacagct gggtgtcccg gggtgagcct ctcagcccct 420 cgttcagcct cagttccaca tgtgtaaatg gaggtctagt agctacctca cagggcagtt 480 gttgaaaata agctaatgct cctaaaaccc tgagaacagt gctctgtgta tgataagtgt 540 tcatagacgt cacattattt atttattttg aaaattcttc ttttagtcaa acttataagt 600 tttctgtggc tcaaaatatt ctcaaccagg gtttctttag tggccatcag ctcccagggg 660 gtgatatcat ggaagctgtt atgcttagga atttgtttaa aaagacgtcc tgccctgtgc 720 cccagtacat ttcaacacca cccagccaca cagccgcctt ctggcccaac actcttaaag 780 acacagtgct tgggaaatgt cctcatgccc cctttcctga ggcaggtttg ccactgtttc 840 cccaggcctg gcagtcacag atggcagtna ctgacctgct gtggatttga gagatggaga 900 gaaaacctcc actcttctta ttctcccaat agctcagtct ctgcctcagt tccaatttcc 960 ctttggcgta actatgattg tcgtccaagg cccccctaga taggcaagac tcatgatacc 1020 caaggggtga tcaggggata gagatgagat gtctgggtgg atggcggaat ggggtatttt 1080 ctaactaatg gggtgcaggg gtacctgagc ctgctctcaa atgtgttata cccctaaaaa 1140 atgtttttaa ggtagtgggt tgatataaca gttgttaaga ccatgatgct agaggcaaga 1200 tcgtgagatc catggagaag gtagtggaag gggtagggcc tttattcaca tatatgctgc 1260 cttctccccc aactgatgtg atatccttta tattcgtgac tccagtgaac ccacgcctcg 1320 gaggatttac accctgtatt ggtactcctc ttgagtctgg gctggcctgt gactttaatc 1380 agtgcaaggc ggaagtgggt tcagtgccag ttctaagact acaaagagaa agaaaagttc 1440 aaccttccaa tatcccagca gacatcaggc cccagctgtg tcaccagctt cacgcccacg 1500 agtgaccaca acaaacccag cagaaccaac cagcgcatcc cagccctggt tgcagaatca 1560 tgagtaaata aaatggttgc tgttccaaaa aaaaaaaaaa aaaaaaaaaa aaaaaa 1616 <210> SEQ ID NO 64 <211> LENGTH: 97 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 64 Met Glu Lys Val Val Glu Gly Val Gly Pro Leu Phe Thr Tyr Met Leu 1 5 10 15 Pro Ser Pro Pro Thr Asp Val Ile Ser Phe Ile Phe Val Thr Pro Val 20 25 30 Asn Pro Arg Leu Gly Gly Phe Thr Pro Cys Ile Gly Thr Pro Leu Glu 35 40 45 Ser Gly Leu Ala Cys Asp Phe Asn Gln Cys Lys Ala Glu Val Gly Ser 50 55 60 Val Pro Val Leu Arg Leu Gln Arg Glu Arg Lys Val Gln Pro Ser Asn 65 70 75 80 Ile Pro Ala Asp Ile Arg Pro Gln Leu Cys His Gln Leu His Ala His 85 90 95 Glu <210> SEQ ID NO 65 <211> LENGTH: 937 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 65 gattgccgga agctgaaggg atgctttgaa cgtggggggg ctgcgtcaca gttggactcc 60 cacttgcaga ggacctgatt atgtccagtg accacctgaa caacagcaca ctgaaggagg 120 ctcagttcaa agacctgttc ttaaaaaaag cggagctgga gttcgcccaa atcatcatca 180 tcgtcgtggt ggtcacggtg atggtggtgg tcatcgtctg cctgctgaac cactacaaag 240 tctccacgcg gtccttcatc aaccgcccga accagagccg gaggcgggag gacgggctgc 300 cgcaggaagg gtgcctgtgg ccttcagaca gcgccgcacc gcgctggggc gcctcggaga 360 tcatgcatgc cccgcggtcc agggacaggt tcacagcgcc gtccttcatc cagagggatc 420 gcttcagccg cttccagccc acctacccct atgtgcagca cgagattgat cttcctccca 480 ccatctccct gtccgacggt gaagagccac ctccttacca ggggccctgc accctgcagc 540 tccgggaccc tgaacagcag atggaactca accgagagtc cgtgagggcc ccacccaacc 600 gaaccatatt tgacagtgat ttaatagaca ttgctatgta tagcgggggt ccatgcccac 660 ccagcagcaa ctcgggcatc agtgcaagca cctgcagcag taacgggagg atggaggggc 720 caccccccac atacagcgag gtgatgggcc accacccagg cgcctctttc ctccatcacc 780 agcgcagcaa cgcacacagg ggcagcagac tgcagtttca gcagaacaat gcagagagca 840 caatagtacc catcaaaggc aaagatagga agcctgggaa cctggtctga ttccttccaa 900 cgtgcacttc agctggagaa agaaaccaag aagggaa 937 <210> SEQ ID NO 66 <211> LENGTH: 269 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 66 Met Ser Ser Asp His Leu Asn Asn Ser Thr Leu Lys Glu Ala Gln Phe 1 5 10 15 Lys Asp Leu Phe Leu Lys Lys Ala Glu Leu Glu Phe Ala Gln Ile Ile 20 25 30 Ile Ile Val Val Val Val Thr Val Met Val Val Val Ile Val Cys Leu 35 40 45 Leu Asn His Tyr Lys Val Ser Thr Arg Ser Phe Ile Asn Arg Pro Asn 50 55 60 Gln Ser Arg Arg Arg Glu Asp Gly Leu Pro Gln Glu Gly Cys Leu Trp 65 70 75 80 Pro Ser Asp Ser Ala Ala Pro Arg Trp Gly Ala Ser Glu Ile Met His 85 90 95 Ala Pro Arg Ser Arg Asp Arg Phe Thr Ala Pro Ser Phe Ile Gln Arg 100 105 110 Asp Arg Phe Ser Arg Phe Gln Pro Thr Tyr Pro Tyr Val Gln His Glu 115 120 125 Ile Asp Leu Pro Pro Thr Ile Ser Leu Ser Asp Gly Glu Glu Pro Pro 130 135 140 Pro Tyr Gln Gly Pro Cys Thr Leu Gln Leu Arg Asp Pro Glu Gln Gln 145 150 155 160 Met Glu Leu Asn Arg Glu Ser Val Arg Ala Pro Pro Asn Arg Thr Ile 165 170 175 Phe Asp Ser Asp Leu Ile Asp Ile Ala Met Tyr Ser Gly Gly Pro Cys 180 185 190 Pro Pro Ser Ser Asn Ser Gly Ile Ser Ala Ser Thr Cys Ser Ser Asn 195 200 205 Gly Arg Met Glu Gly Pro Pro Pro Thr Tyr Ser Glu Val Met Gly His 210 215 220 His Pro Gly Ala Ser Phe Leu His His Gln Arg Ser Asn Ala His Arg 225 230 235 240 Gly Ser Arg Leu Gln Phe Gln Gln Asn Asn Ala Glu Ser Thr Ile Val 245 250 255 Pro Ile Lys Gly Lys Asp Arg Lys Pro Gly Asn Leu Val 260 265 <210> SEQ ID NO 67 <211> LENGTH: 1467 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 67 ttttacaggt agaataaaca tagcatttcc ttctgtagac agaaggtgat atagttaacc 60 tcatgcactt tcatccacta agactccaag tcaaatgcca ccacactgca gcacacccaa 120 gagagcctgg tctacctgct tccaggagtt cacacgatgt acaggaaaag gcactaagta 180 aatttaactt tccattattt ttttttctgg agttatttct tattgtacaa agatttccag 240 acaactcctt ttccatttca ttcattgcca tttctgcttt atccagcagc acggagcctc 300 agctttgaga aatctcttga ccagagtgat ttttattttc ctcacacata aaatgtatgg 360 aaatggagat atctttttgg gcatatcagg gctatcatga gaagataaag ccatcaagct 420 gtaataatgg ttatgaaagc acttccaaca attctaaaga tgataaaaca gtggatgatc 480 cactgttgca caaaattcta gcaacaaatt ctaattcagc cacacttgtt cttaataaca 540 gattgctctg tttttcataa ttattctaca tattaatatc actgtgaagt cattacaaca 600 gctgtgtttt tttggtcaca gatgttttat tttcaaagaa aacaaaattg tgtacgtttt 660 tttccttgga gttctgattg aaccagtttt atatctaaag aaatacagaa atatctattc 720 ttgcctatcc atgatgtaca gccattatca aagtcttata agttaatctt ttttcaatca 780 tagtttattc cttttggtat taaaaaaatc ctatttacag acagtgcaaa actgatagaa 840 aagtaggaag agagaaaatt aaatagccaa ttagaaaaat actgtagaat tgcagttcca 900 gagtatggat aggatatcat agcaagctgt tgagtaaggc gaggaaggct tctctgagga 960 ggtgaccatc aactgagaga gggtttatag aatgagaaat gtaaggaata taaggaagct 1020 gtggtgcggg aaagaatatg tgcggcaaca agaggacaat actgtagggt tcgtagacca 1080 tcaatctggt accatttctg gagccattaa ttctttatat gagggtaagt ttaagacagg 1140 cttgtggctg ggcacagtgg ctcatgcctg taatcccagc actttggaag gccgaagcgg 1200 gctgatcacc tgaggtcagg aatttgagaa cagcctggcc aacatggtga cacccatctc 1260 tactaaatat acaaaattag ccgggtgtgg tggtgggagc ctgtaatccc agctactcgt 1320 aaggctgagg caggagaatt gcatgaaccc aggaggtgga ggttgcagtg agccgagatt 1380 gtgccactgt cccactgtcc tccagcctgg gccacagagt gatactctgc ctcaccaaaa 1440 aaaaaaaaaa aaaaaaaaaa aaaaaaa 1467 <210> SEQ ID NO 68 <211> LENGTH: 81 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 68 Met His Phe His Pro Leu Arg Leu Gln Val Lys Cys His His Thr Ala 1 5 10 15 Ala His Pro Arg Glu Pro Gly Leu Pro Ala Ser Arg Ser Ser His Asp 20 25 30 Val Gln Glu Lys Ala Leu Ser Lys Phe Asn Phe Pro Leu Phe Phe Phe 35 40 45 Leu Glu Leu Phe Leu Ile Val Gln Arg Phe Pro Asp Asn Ser Phe Ser 50 55 60 Ile Ser Phe Ile Ala Ile Ser Ala Leu Ser Ser Ser Thr Glu Pro Gln 65 70 75 80 Leu <210> SEQ ID NO 69 <211> LENGTH: 1235 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 69 tttctccttt cctctccctg tgcctcatct tcctctcctc tctctctccc ttctctcttc 60 tccgtttctc tttttcaccc cactccttca tcttgtctcg ctgtctatat tgttttcctt 120 ctctgtatct tcattgcctt tgctttcttt caaactttct ccttcacaga tttttcttta 180 ttaatcagaa tcatactgac caacatgtgc tgaggacttt ctgtgtgctc tgtgcttcac 240 atacagtcat gtgcatcttt ccagttccac aagtgagtta tcctcatttc tcggggccat 300 agagctagtg agtgacagag ctaggttttg tatgtcaaag cctctgtcct acatgacatg 360 gcttttcctg ctgccttctc ccctggtatt cgtctccctc ttttctcctc tggctctgct 420 ggctctcctc tggctctgcg agggggtggt tttcagcctg ggcccttgca gatgtgtctg 480 tggcagcagg ccacacagac cgcagcgggc tgggcagcgt cctgagagac ctagtgaagc 540 caggcgacga gaaccttcgg gagatgaaca agaagctgca gaacatgctg gaggagcagc 600 tcaccaagaa tatgcacttg cacaaggata tggaagttct gtcccaggaa attgtgcggc 660 tcagcaagga gtgcgtgggg cctcctgacc cagacctaga gccaggagaa accagctaaa 720 gacctgcagg ctgcacccac ctcctcccct tcctaccccc taggatgcta tttcccttgg 780 gctgtggtgg aaaaatgagg gctggagcca aaatcaaata gcttgggaga ctggacatta 840 aaggggctag aggcctgatg gttagtgtta atgatcctgt cttagggcag aggccaccag 900 ggagtgggga tcctgaggga aggggcaggg atttctcctt cttcttggtc ctggctccca 960 agggcttctg tcttcatctc tgcatgagct ctccttccca gagaccaact cttttttatt 1020 ttattttatt ttatttttta atttatgtct ggagcctggc tactctgcat ttgggattgg 1080 ggatgctggg tgggtgtgtg gtccatgttc agcgttctag caacacgtgt gtgtgtgtgt 1140 gtgtaaaggc tatgcagcca aaataccatc tggccagacg ggcccacccc aaaaaaaaaa 1200 aaaggaaaaa aaaaaaaaaa aaaaaaaaaa aaaaa 1235 <210> SEQ ID NO 70 <211> LENGTH: 118 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 70 Met Ser Lys Pro Leu Ser Tyr Met Thr Trp Leu Phe Leu Leu Pro Ser 1 5 10 15 Pro Leu Val Phe Val Ser Leu Phe Ser Pro Leu Ala Leu Leu Ala Leu 20 25 30 Leu Trp Leu Cys Glu Gly Val Val Phe Ser Leu Gly Pro Cys Arg Cys 35 40 45 Val Cys Gly Ser Arg Pro His Arg Pro Gln Arg Ala Gly Gln Arg Pro 50 55 60 Glu Arg Pro Ser Glu Ala Arg Arg Arg Glu Pro Ser Gly Asp Glu Gln 65 70 75 80 Glu Ala Ala Glu His Ala Gly Gly Ala Ala His Gln Glu Tyr Ala Leu 85 90 95 Ala Gln Gly Tyr Gly Ser Ser Val Pro Gly Asn Cys Ala Ala Gln Gln 100 105 110 Gly Val Arg Gly Ala Ser 115 <210> SEQ ID NO 71 <211> LENGTH: 835 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 71 gggggaaaag ggcggaaaag gacaaggatc caaactggcg aatttgctga tcttcgcgtc 60 cctctccgct ttccggccgg cagcgctgcc agggtatatt tccttttttc cgatcctgca 120 acagcctctt taaactgttt aaatgagaat gtccttggct cagagagtac tactcacctg 180 gcttttcaca ctactcttct tgatcatgtt ggtgttgaaa ctggatgaga aagcaccttg 240 gaactggttc ctcatattta ttccagtctg gatatttgat actatccttc ttgtcctgct 300 gattgtgaaa atggctgggc ggtgtaagtc tggctttgac cctcgacatg gatcacacaa 360 tattaaaaaa aaagcctggt acctcattgc aatgttactt aaattagcct tctgcctcgc 420 actctgtgct aaactggaac agtttactac catgaatcta tcctatgtct tcattccttt 480 atgggccttg ctggctgggg cttaaacaga actcggatat aatgtctttt gtgagagaga 540 ctgacttcta agtacatcat ctcctttcta ttgcggttca acaagttacc attaaagtgt 600 tctgaatctg tcaagcttca agaataccag agaactgagg ggaaatacca aaggtagttt 660 tatactactt ccataaaaca agattggtga atcacggact tctagtcaac ctacagctta 720 attattcagc atttgagtta ttgagatccc tattatctct agggaaataa agtttgtttt 780 ggacctcaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaa 835 <210> SEQ ID NO 72 <211> LENGTH: 120 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 72 Met Arg Met Ser Leu Ala Gln Arg Val Leu Leu Thr Trp Leu Phe Thr 1 5 10 15 Leu Leu Phe Leu Ile Met Leu Val Leu Lys Leu Asp Glu Lys Ala Pro 20 25 30 Trp Asn Trp Phe Leu Ile Phe Ile Pro Val Trp Ile Phe Asp Thr Ile 35 40 45 Leu Leu Val Leu Leu Ile Val Lys Met Ala Gly Arg Cys Lys Ser Gly 50 55 60 Phe Asp Pro Arg His Gly Ser His Asn Ile Lys Lys Lys Ala Trp Tyr 65 70 75 80 Leu Ile Ala Met Leu Leu Lys Leu Ala Phe Cys Leu Ala Leu Cys Ala 85 90 95 Lys Leu Glu Gln Phe Thr Thr Met Asn Leu Ser Tyr Val Phe Ile Pro 100 105 110 Leu Trp Ala Leu Leu Ala Gly Ala 115 120 <210> SEQ ID NO 73 <211> LENGTH: 1287 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 73 ccgaggcggg aggatgaagt tgattgacta tggtctctcc ggctaccagg aagagtctgc 60 cgaaggtgaa ggccatggac ttcatcacct ccacagccat cctgcccctg ctgttcggct 120 gcctgggcgt cttcggcctc ttccggctgc tgcagtgggt gcgcgggaag gcctacctgc 180 ggaatgctgt ggtggtgatc acaggcgcca cctcagggct gggcaaagaa tgtgcaaaag 240 tcttctatgc tgcgggtgct aaactggtgc tctgtggccg gaatggtggg gccctagaag 300 agctcatcag agaactcacc gcttctcatg ccaccaaggt gcagacacac aagccttact 360 tggtgacctt cgacctcaca gactctgggg ccatagttgc agcagcagct gagatcctgc 420 agtgctttgg ctatgtcgac atacttgtca acaatgctgg gatcagctac cgtggtacca 480 tcatggacac cacagtggat gtggacaaga gggtcatgga gacaaactac tttggcccag 540 ttgctctaac gaaagcactc ctgccctcca tgatcaagag gaggcaaggc cacattgtcg 600 ccatcagcag catccagggc aagatgagca ttccttttcg atcagcatat gcagcctcca 660 agcacgcaac ccaggctttc tttgactgtc tgcgtgccga gatggaacag tatgaaattg 720 aggtgaccgt catcagcccc ggctacatcc acaccaacct ctctgtaaat gccatcaccg 780 cggatggatc taggtatgga gttatggaca ccaccacagc ccagggccga agccctgtgg 840 aggtggccca ggatgttctt gctgctgtgg ggaagaagaa gaaagatgtg atcctggctg 900 acttactgcc ttccttggct gtttatcttc gaactctggc tcctgggctc ttcttcagcc 960 tcatggcctc cagggccaga aaagagcgga aatccaagaa ctcctagtac tctgaccagc 1020 cagggccagg gcagagaagc agcactctta ggcttgctta ctctacaagg gacagttgca 1080 tttgttgaga ctttaatgga gatttttctc acaagtggga aagactgaag aaacacatct 1140 cgtgcagatc tgctggcaga ggacaatcaa aaacgacaac aagcttcttc ccagggtgag 1200 gggaaacact taaggaataa atatggagct ggggtttaac actaaaacta gaaataaaca 1260 tctcaaacag taaaaaaaaa aaaaaaa 1287 <210> SEQ ID NO 74 <211> LENGTH: 325 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 74 Met Val Ser Pro Ala Thr Arg Lys Ser Leu Pro Lys Val Lys Ala Met 1 5 10 15 Asp Phe Ile Thr Ser Thr Ala Ile Leu Pro Leu Leu Phe Gly Cys Leu 20 25 30 Gly Val Phe Gly Leu Phe Arg Leu Leu Gln Trp Val Arg Gly Lys Ala 35 40 45 Tyr Leu Arg Asn Ala Val Val Val Ile Thr Gly Ala Thr Ser Gly Leu 50 55 60 Gly Lys Glu Cys Ala Lys Val Phe Tyr Ala Ala Gly Ala Lys Leu Val 65 70 75 80 Leu Cys Gly Arg Asn Gly Gly Ala Leu Glu Glu Leu Ile Arg Glu Leu 85 90 95 Thr Ala Ser His Ala Thr Lys Val Gln Thr His Lys Pro Tyr Leu Val 100 105 110 Thr Phe Asp Leu Thr Asp Ser Gly Ala Ile Val Ala Ala Ala Ala Glu 115 120 125 Ile Leu Gln Cys Phe Gly Tyr Val Asp Ile Leu Val Asn Asn Ala Gly 130 135 140 Ile Ser Tyr Arg Gly Thr Ile Met Asp Thr Thr Val Asp Val Asp Lys 145 150 155 160 Arg Val Met Glu Thr Asn Tyr Phe Gly Pro Val Ala Leu Thr Lys Ala 165 170 175 Leu Leu Pro Ser Met Ile Lys Arg Arg Gln Gly His Ile Val Ala Ile 180 185 190 Ser Ser Ile Gln Gly Lys Met Ser Ile Pro Phe Arg Ser Ala Tyr Ala 195 200 205 Ala Ser Lys His Ala Thr Gln Ala Phe Phe Asp Cys Leu Arg Ala Glu 210 215 220 Met Glu Gln Tyr Glu Ile Glu Val Thr Val Ile Ser Pro Gly Tyr Ile 225 230 235 240 His Thr Asn Leu Ser Val Asn Ala Ile Thr Ala Asp Gly Ser Arg Tyr 245 250 255 Gly Val Met Asp Thr Thr Thr Ala Gln Gly Arg Ser Pro Val Glu Val 260 265 270 Ala Gln Asp Val Leu Ala Ala Val Gly Lys Lys Lys Lys Asp Val Ile 275 280 285 Leu Ala Asp Leu Leu Pro Ser Leu Ala Val Tyr Leu Arg Thr Leu Ala 290 295 300 Pro Gly Leu Phe Phe Ser Leu Met Ala Ser Arg Ala Arg Lys Glu Arg 305 310 315 320 Lys Ser Lys Asn Ser 325 <210> SEQ ID NO 75 <211> LENGTH: 1396 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 75 cggaggaggt ggcggcgctg gagctcctcc cggggaccag cgacccgggg agcgagcacg 60 tcgctccgca ccgctcttcc tccagccgct gagccgtccc ttctcgccat gtcccagagc 120 aggcaccgcg ccgaggcccc gccgctggag cgcgaggaca gtgggacctt cagtttgggg 180 aagatgataa cagctaagcc agggaaaaca ccgattcagg tattacacga atacggcatg 240 aagaccaaga acatcccagt ttatgaatgt gaaagatctg atgtgcaaat acacgtgccc 300 actttcacct tcagagtaac cgttggtgac ataacctgca caggtgaagg tacaagtaag 360 aagctggcga aacatagagc tgcagaggct gccataaaca ttttgaaagc caatgcaagt 420 atttgctttg cagttcctga ccccttaatg cctgaccctt ccaagcaacc aaagaaccag 480 cttaatccta ttggttcatt acaggaattg gctattcatc atggctggag acttcctgaa 540 tatacccttt cccaggaggg aggacctgct cataagagag aatatactac aatttgcagg 600 ctagagtcat ttatggaaac tggaaagggg gcatcaaaaa agcaagccaa aaggaatgct 660 gctgagaaat ttcttgccaa atttagtaat atttctccag agaaccacat ttctttaaca 720 aatgtagtag gacattcttt aggatgtact tggcattcct tgaggaattc tcctggtgaa 780 aagatcaact tactgaaaag aagcctcctt agtattccaa atacagatta catccagctg 840 cttagtgaaa ttgccaagga acaaggtttt aatataacat atttggatat agatgaactg 900 agcgccaatg gacaatatca atgtcttgct gaactgtcca ccagccccat cacagtctgt 960 catggctccg gtatctcctg tggcaatgca caaagtgatg cagctcacaa tgctttgcag 1020 tatttaaaga taatagcaga aagaaagtaa atctggagca acttaaaaaa tctttcagta 1080 gcacataaaa agttcccctc tggccccttc ccaagtaaaa cttttaccgt agtgtttatg 1140 tcttgtttct aaatctcttc atagattcca tcaacactcc agatttaatt atctcctcat 1200 agttgttatt aagctctttt taatggcttc aactttgtat cagtatactg tatttataaa 1260 ctttgtacca caagagagag tgtagcaccc attttacagt gccatgcaca tcagagaaag 1320 aaactgcatg tttgttgttg atgatgaaat aaaaatgcta gcgacagtca aaaaaaaaaa 1380 aaaaaaaaaa aaaaaa 1396 <210> SEQ ID NO 76 <211> LENGTH: 313 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 76 Met Ser Gln Ser Arg His Arg Ala Glu Ala Pro Pro Leu Glu Arg Glu 1 5 10 15 Asp Ser Gly Thr Phe Ser Leu Gly Lys Met Ile Thr Ala Lys Pro Gly 20 25 30 Lys Thr Pro Ile Gln Val Leu His Glu Tyr Gly Met Lys Thr Lys Asn 35 40 45 Ile Pro Val Tyr Glu Cys Glu Arg Ser Asp Val Gln Ile His Val Pro 50 55 60 Thr Phe Thr Phe Arg Val Thr Val Gly Asp Ile Thr Cys Thr Gly Glu 65 70 75 80 Gly Thr Ser Lys Lys Leu Ala Lys His Arg Ala Ala Glu Ala Ala Ile 85 90 95 Asn Ile Leu Lys Ala Asn Ala Ser Ile Cys Phe Ala Val Pro Asp Pro 100 105 110 Leu Met Pro Asp Pro Ser Lys Gln Pro Lys Asn Gln Leu Asn Pro Ile 115 120 125 Gly Ser Leu Gln Glu Leu Ala Ile His His Gly Trp Arg Leu Pro Glu 130 135 140 Tyr Thr Leu Ser Gln Glu Gly Gly Pro Ala His Lys Arg Glu Tyr Thr 145 150 155 160 Thr Ile Cys Arg Leu Glu Ser Phe Met Glu Thr Gly Lys Gly Ala Ser 165 170 175 Lys Lys Gln Ala Lys Arg Asn Ala Ala Glu Lys Phe Leu Ala Lys Phe 180 185 190 Ser Asn Ile Ser Pro Glu Asn His Ile Ser Leu Thr Asn Val Val Gly 195 200 205 His Ser Leu Gly Cys Thr Trp His Ser Leu Arg Asn Ser Pro Gly Glu 210 215 220 Lys Ile Asn Leu Leu Lys Arg Ser Leu Leu Ser Ile Pro Asn Thr Asp 225 230 235 240 Tyr Ile Gln Leu Leu Ser Glu Ile Ala Lys Glu Gln Gly Phe Asn Ile 245 250 255 Thr Tyr Leu Asp Ile Asp Glu Leu Ser Ala Asn Gly Gln Tyr Gln Cys 260 265 270 Leu Ala Glu Leu Ser Thr Ser Pro Ile Thr Val Cys His Gly Ser Gly 275 280 285 Ile Ser Cys Gly Asn Ala Gln Ser Asp Ala Ala His Asn Ala Leu Gln 290 295 300 Tyr Leu Lys Ile Ile Ala Glu Arg Lys 305 310 <210> SEQ ID NO 77 <211> LENGTH: 1238 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 77 tccgcggatt cccagcttga gaaacacctc tttgccccgt catgccaaag aggaaagtga 60 ccttccaagg cgtgggagat gaggaggatg aggatgaaat cattgtcccc aagaagaagc 120 tggtggaccc tgtggctggg tcagggggtc ctgggagccg ctttaaaggc aaacactctt 180 tggatagcga tgaggaggag gatgatgatg atggggggtc cagcaaatat gacatcttgg 240 cctcagagga tgtagaaggt caggaggcag ccacactccc cagcgagggg ggtgttcgga 300 tcacaccctt taacctgcag gaggagatgg aggaaggcca ctttgatgcc gatggcaact 360 acttcctgaa ccgggatgct cagatccgag acagctggct ggacaacatt gactgggtga 420 agatccggga gcggccacct ggccagcgcc aggcctcaga ctcggaggag gaggacagct 480 tgggccagac ctcaatgagt gcccaagccc tcttggaggg acttttggag ctcctattgc 540 ctagagagac agtggctggg gcactgaggc gtctgggggc ccgaggagga ggcaaaggga 600 gaaaggggcc tgggcaaccc agttcccctc agcgcctgga ccggctctcc gggttggccg 660 accagatggt ggcccggggc aaccttggtg tgtaccagga aacaagggaa cggttggcta 720 tgcgtctgaa gggtttgggg tgtcagaccc taggacccca caatcccaca cccccaccct 780 ccctggacat gttcgctgag gagttggcgg aggaggaact ggagacccca acccctaccc 840 agagaggaga agcagagtcg cggggagatg gtctggtgga tgtgatgtgg gaatataagt 900 gggagaacac gggggatgcc gagctgtatg ggcccttcac cagcgcccag atgcagaccg 960 gggtgagtga aggctacttc ccggacggtg tttattgccg gaagctgggc ccccctgggg 1020 gtcagttcta caactccaaa cgcattgacg ttgacctcta caccggagcc ggctgggggc 1080 ccagtttggt gggcccttct ttcctggact ttgtggagga ggcgccaagt gtctcaggca 1140 gcgcaggaaa ttggaggcca tttttcagtc aatttccctt tcccaataaa agcctttagt 1200 tgtgtaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaa 1238 <210> SEQ ID NO 78 <211> LENGTH: 385 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 78 Met Pro Lys Arg Lys Val Thr Phe Gln Gly Val Gly Asp Glu Glu Asp 1 5 10 15 Glu Asp Glu Ile Ile Val Pro Lys Lys Lys Leu Val Asp Pro Val Ala 20 25 30 Gly Ser Gly Gly Pro Gly Ser Arg Phe Lys Gly Lys His Ser Leu Asp 35 40 45 Ser Asp Glu Glu Glu Asp Asp Asp Asp Gly Gly Ser Ser Lys Tyr Asp 50 55 60 Ile Leu Ala Ser Glu Asp Val Glu Gly Gln Glu Ala Ala Thr Leu Pro 65 70 75 80 Ser Glu Gly Gly Val Arg Ile Thr Pro Phe Asn Leu Gln Glu Glu Met 85 90 95 Glu Glu Gly His Phe Asp Ala Asp Gly Asn Tyr Phe Leu Asn Arg Asp 100 105 110 Ala Gln Ile Arg Asp Ser Trp Leu Asp Asn Ile Asp Trp Val Lys Ile 115 120 125 Arg Glu Arg Pro Pro Gly Gln Arg Gln Ala Ser Asp Ser Glu Glu Glu 130 135 140 Asp Ser Leu Gly Gln Thr Ser Met Ser Ala Gln Ala Leu Leu Glu Gly 145 150 155 160 Leu Leu Glu Leu Leu Leu Pro Arg Glu Thr Val Ala Gly Ala Leu Arg 165 170 175 Arg Leu Gly Ala Arg Gly Gly Gly Lys Gly Arg Lys Gly Pro Gly Gln 180 185 190 Pro Ser Ser Pro Gln Arg Leu Asp Arg Leu Ser Gly Leu Ala Asp Gln 195 200 205 Met Val Ala Arg Gly Asn Leu Gly Val Tyr Gln Glu Thr Arg Glu Arg 210 215 220 Leu Ala Met Arg Leu Lys Gly Leu Gly Cys Gln Thr Leu Gly Pro His 225 230 235 240 Asn Pro Thr Pro Pro Pro Ser Leu Asp Met Phe Ala Glu Glu Leu Ala 245 250 255 Glu Glu Glu Leu Glu Thr Pro Thr Pro Thr Gln Arg Gly Glu Ala Glu 260 265 270 Ser Arg Gly Asp Gly Leu Val Asp Val Met Trp Glu Tyr Lys Trp Glu 275 280 285 Asn Thr Gly Asp Ala Glu Leu Tyr Gly Pro Phe Thr Ser Ala Gln Met 290 295 300 Gln Thr Gly Val Ser Glu Gly Tyr Phe Pro Asp Gly Val Tyr Cys Arg 305 310 315 320 Lys Leu Gly Pro Pro Gly Gly Gln Phe Tyr Asn Ser Lys Arg Ile Asp 325 330 335 Val Asp Leu Tyr Thr Gly Ala Gly Trp Gly Pro Ser Leu Val Gly Pro 340 345 350 Ser Phe Leu Asp Phe Val Glu Glu Ala Pro Ser Val Ser Gly Ser Ala 355 360 365 Gly Asn Trp Arg Pro Phe Phe Ser Gln Phe Pro Phe Pro Asn Lys Ser 370 375 380 Leu 385 <210> SEQ ID NO 79 <211> LENGTH: 1558 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1488..1489) <400> SEQUENCE: 79 cttctgtgcc gggggtcttc ctgctgtcat gaaggacgta ccgggcttcc tacagcagag 60 ccagaactcc gggcccgggc agcccgctgt gtggcaccgt ctggaggagc tctacacgaa 120 gaagttgtgg catcagctga cacttcaggt gcttgatttt gtgcaggatc cgtgctttgc 180 ccaaggagat ggtctcatta agctttatga aaactttatc agtgaatttg aacacagggt 240 gaaccctttg tccctcgtgg aaatcattct tcatgtagtt agacagatga ctgatcctaa 300 tgtggctctt acttttctgg aaaagactcg tgagaaggtg aaaagtagtg atgaggcagt 360 gatcctgtgt aaaacagcaa ttggagctct aaaattaaac atcggggacc tacaggttac 420 aaaggaaaca attgaagatg ttgaagaaat gctcaacaac cttcctggtg tgacatcggt 480 tcacagtcgt ttctatgatc tctccagtaa atactatcaa acaatcggaa accacgcgtc 540 ctactacaaa gatgctctgc ggtttttggg ctgtgttgac atcaaggatc taccagtgtc 600 tgagcagcag gagagagcct tcacgctggg gctagcagga cttctcggcg agggagtttt 660 taactttgga gaactcctca tgcaccctgt gctggagtcc ctgaggaata ctgaccggca 720 gtggctgatt gacaccctct atgccttcaa cagtggcaac gtagagcggt tccagactct 780 gaagactgcc tggggccagc agcctgattt agcagctaat gaagcccagc ttctgaggaa 840 aattcagttg ttgtgcctca tggagatgac tttcacacga cctgccaatc acagacaact 900 cacttttgaa gaaattgcca aaagtgctaa aatcacagtg aatgaggtgg agcttctggt 960 gatgaaggcc ctttcggtgg ggctggtgaa aggcagtata gacgaggtgg acaaacgagt 1020 ccacatgacc tgggtgcagc cccgagtgtt ggatttgcaa cagatcaagg gaatgaagga 1080 ccgcctggag ttctggtgca cggatgtgaa gagcatggag atgctggtgg agcaccaggc 1140 ccatgacatc ctcacctagg gccccctggt tccccgtcgt gtctcctttg actcacctga 1200 gagaggcgtt tgcagccaat gaagctggct gctcagacgg tcgacattga atttgggtgg 1260 gggttgggat cctgtctgaa gtacagactg ttcttgctct aaaaacagga ctgtccctga 1320 tgggagccag gccacaggga ggaggcttct ttgtgggtct ctcctgcaga gggtgggggt 1380 ctcagggtct taggtgatac gggagagaaa gaacgtgcca ggcaggaggc cccctgaagt 1440 ctgtgtactc cgaggtggat ctccatcccc atccacctgt acggacannt tttccgttgc 1500 ggtttgagaa tgttcctata ataaacccct ctgctttgtt cttaaaaaaa aaaaaaaa 1558 <210> SEQ ID NO 80 <211> LENGTH: 376 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 80 Met Lys Asp Val Pro Gly Phe Leu Gln Gln Ser Gln Asn Ser Gly Pro 1 5 10 15 Gly Gln Pro Ala Val Trp His Arg Leu Glu Glu Leu Tyr Thr Lys Lys 20 25 30 Leu Trp His Gln Leu Thr Leu Gln Val Leu Asp Phe Val Gln Asp Pro 35 40 45 Cys Phe Ala Gln Gly Asp Gly Leu Ile Lys Leu Tyr Glu Asn Phe Ile 50 55 60 Ser Glu Phe Glu His Arg Val Asn Pro Leu Ser Leu Val Glu Ile Ile 65 70 75 80 Leu His Val Val Arg Gln Met Thr Asp Pro Asn Val Ala Leu Thr Phe 85 90 95 Leu Glu Lys Thr Arg Glu Lys Val Lys Ser Ser Asp Glu Ala Val Ile 100 105 110 Leu Cys Lys Thr Ala Ile Gly Ala Leu Lys Leu Asn Ile Gly Asp Leu 115 120 125 Gln Val Thr Lys Glu Thr Ile Glu Asp Val Glu Glu Met Leu Asn Asn 130 135 140 Leu Pro Gly Val Thr Ser Val His Ser Arg Phe Tyr Asp Leu Ser Ser 145 150 155 160 Lys Tyr Tyr Gln Thr Ile Gly Asn His Ala Ser Tyr Tyr Lys Asp Ala 165 170 175 Leu Arg Phe Leu Gly Cys Val Asp Ile Lys Asp Leu Pro Val Ser Glu 180 185 190 Gln Gln Glu Arg Ala Phe Thr Leu Gly Leu Ala Gly Leu Leu Gly Glu 195 200 205 Gly Val Phe Asn Phe Gly Glu Leu Leu Met His Pro Val Leu Glu Ser 210 215 220 Leu Arg Asn Thr Asp Arg Gln Trp Leu Ile Asp Thr Leu Tyr Ala Phe 225 230 235 240 Asn Ser Gly Asn Val Glu Arg Phe Gln Thr Leu Lys Thr Ala Trp Gly 245 250 255 Gln Gln Pro Asp Leu Ala Ala Asn Glu Ala Gln Leu Leu Arg Lys Ile 260 265 270 Gln Leu Leu Cys Leu Met Glu Met Thr Phe Thr Arg Pro Ala Asn His 275 280 285 Arg Gln Leu Thr Phe Glu Glu Ile Ala Lys Ser Ala Lys Ile Thr Val 290 295 300 Asn Glu Val Glu Leu Leu Val Met Lys Ala Leu Ser Val Gly Leu Val 305 310 315 320 Lys Gly Ser Ile Asp Glu Val Asp Lys Arg Val His Met Thr Trp Val 325 330 335 Gln Pro Arg Val Leu Asp Leu Gln Gln Ile Lys Gly Met Lys Asp Arg 340 345 350 Leu Glu Phe Trp Cys Thr Asp Val Lys Ser Met Glu Met Leu Val Glu 355 360 365 His Gln Ala His Asp Ile Leu Thr 370 375 <210> SEQ ID NO 81 <211> LENGTH: 1257 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1201) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1204) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1206) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1215) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1217) <400> SEQUENCE: 81 ccagctctgg tatcgtaaat gtttgtagcc aatacaacat ccctggttat gatagaagga 60 tgcccttgac tggcccagct ctggtatcct aaatgttcgg agccgatata acatccctgg 120 ttatgataga aggatgcctt ttcttagacg tgaggatgcg tcccacgggc ttcagcactg 180 ggtctgctct gtggaacttc caggccgaag ctggggaggg taatggggca gcatggctgc 240 aggagtcgag ctcagtgcct gagccgggag ctcgatgcgg gagctgtggg ctgctcctcc 300 tccctgctag gagcaggtgc aagaggcctg cagagtgctg gggctgggca cggacctcac 360 agtgccatga agcctcgtgc agctttgaat ttcacttgtg atttcttcat ggaacttcaa 420 agccctagca atgtaggcgc gtagtcaatt attatttgag taagtgactg cgtgcaatgg 480 cccaggataa gggggttctg gagagggcag tccgtgctcc tattctttct ctgtctactt 540 tattatgatt tttgcttttt actatgaaaa attttaagcc ttcagaaaag tagagtgata 600 tgccacccat atacctatta tctagattta agaagaagaa tgattttcca tctgttattt 660 gctgtgtttg ggaaggattt taaagtacag acgtcatgac attttacctc taaatgcttc 720 ggatgcaact ctaaaaaata aggatgtttt catacttaac cacattttta tgaatacgct 780 gaacaaagca aatcagttta tttgtccccc aaatattttg atttgttcaa acaagaattc 840 agtcagagtc cccatgatgc gtgtggtggt gcttggtggt gccttagttc ctttgacatg 900 ggacagcccc tcccagctct tcatttctca tgagttgaaa aggctgggcc gggcccgatg 960 ctcacgcctg taatcccagc actttgggag gcgtgaggca ggtggatcac gaggtcagga 1020 gatcgagacc atcctggcta acatggtgaa accctgtctg tactaaaaga atacaaaaaa 1080 ttagccgggt gtggtggcgc gcgcccgtag tccctgctac ctgggaggct gaggcaggag 1140 agtggtgtga acccggcagg cggaaattaa agtgagccga gatcgctctt tgtactcgta 1200 ngtngnggtc agatngngga ctctcgtctc aaaaaaaaaa aaaaaaaaaa aaaaaaa 1257 <210> SEQ ID NO 82 <211> LENGTH: 102 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 82 Met Phe Gly Ala Asp Ile Thr Ser Leu Val Met Ile Glu Gly Cys Leu 1 5 10 15 Phe Leu Asp Val Arg Met Arg Pro Thr Gly Phe Ser Thr Gly Ser Ala 20 25 30 Leu Trp Asn Phe Gln Ala Glu Ala Gly Glu Gly Asn Gly Ala Ala Trp 35 40 45 Leu Gln Glu Ser Ser Ser Val Pro Glu Pro Gly Ala Arg Cys Gly Ser 50 55 60 Cys Gly Leu Leu Leu Leu Pro Ala Arg Ser Arg Cys Lys Arg Pro Ala 65 70 75 80 Glu Cys Trp Gly Trp Ala Arg Thr Ser Gln Cys His Glu Ala Ser Cys 85 90 95 Ser Phe Glu Phe His Leu 100 <210> SEQ ID NO 83 <211> LENGTH: 2520 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 83 ccacctgccg ggtaagggcc cctcgggccg tggtcgggca tcgattggcc ccgcctggcg 60 cagcccccgc ccctgcagcg gactgcggtg ctcatcagac ctgagcagtt gctccggcgg 120 cgctcgggga gggagccagc agcctagggc ctaggcccgg gccaccatgg cgctgcctcc 180 aggcccagcc gccctccggc acacactgct gctcctgcca gcccttctga gctcaggttg 240 gggggagttg gagccacaaa tagatggtca gacctgggct gagcgggcac ttcgggagaa 300 tgaacgccac gccttcacct gccgggtggc aggggggcct ggcaccccca gattggcctg 360 gtatctggat ggacagctgc aggaggccag cacctcaaga ctgctgagcg tgggagggga 420 ggccttctct ggaggcacca gcaccttcac tgtcactgcc catcgggccc agcatgagct 480 caactgctct ctgcaggacc ccagaagtgg ccgatcagcc aacgcctctg tcatccttaa 540 tgtgcaattc aagccagaga ttgcccaagt cggcgccaag taccaggaag ctcagggccc 600 aggcctcctg gttgtcctgt ttgccctggt gcgtgccaac ccgccggcca atgtcacctg 660 gatcgaccag gatgggccag tgactgtcaa cacctctgac ttcctggtgc tggatgcgca 720 gaactacccc tggctcacca accacacggt gcagctgcag ctccgcagcc tggcacacaa 780 cctctcggtg gtggccacca atgacgtggg tgtcaccagt gcgtcgcttc cagccccagg 840 gcttctggct acccgggtgg aagtgccact gctgggcatt gttgtggctg ctgggcttgc 900 actgggcacc ctcgtggggt tcagcacctt ggtggcctgc ctggtctgca gaaaagagaa 960 gaaaaccaaa ggcccctccc ggcacccatc tctgatatca agtgactcca acaacctaaa 1020 actcaacaac gtgcgcctgc cacgggagaa catgtccctc ccgtccaacc ttcagctcaa 1080 tgacctcact ccagattcca gagcagtgaa accagcagac cggcagatgg ctcagaacaa 1140 cagccggcca gagcttctgg acccggagcc cggcggcctc ctcaccagcc aaggtttcat 1200 ccgcctccca gtgctgggct atatctatcg agtgtccagc gtgagcagtg atgagatctg 1260 gctctgagcc gagggcgaga caggagtatt ctcttggcct ctggacaccc tcccattcct 1320 ccaaggcatc ctctacctag ctaggtcacc aacgtgaaga agttatgcca ctgccacttt 1380 tgcttgccct cctggctggg gtgccctcca tgtcatgcac gtgatgcatt tcactgggct 1440 gtaacccgca ggggcacagg tatctttggc aaggctacca gttggacgta agcccctcat 1500 gctgactcag ggtgggccct gcatgtgatg actgggccct tccagaggga gctctttggc 1560 caggggtgtt cagatgtcat ccagcatcca agtgtggcat ggcctgctgt ataccccacc 1620 ccagtactcc acagcacctt gtacagtagg catgggggcg tgcctgtgtg ggggacaggg 1680 agggccctgc atggattttc ctccttccta tgctatgtag ccttgttccc tcaggtaaaa 1740 tttaggaccc tgctagctgt gcagaaccca attgcccttt gcacagaaac caacccctga 1800 cccagcggta ccggccaagc acaaacgtcc tttttgctgc acacgtctct gcccttcact 1860 tcttctcttc tgtcccacct cctcttggga attctaggtt acacgttgga ccttctctac 1920 tacttcactg ggcactagac ttttctattg gcctgtgcca tcgcccagta ttagcacaag 1980 ttagggagga agaggcaggc gatgagtcta gtagcaccca ggacggcttg tagctatgca 2040 tcattttcct acggcgttag cactttaagc acatccctag ggaggggtga gtgagggccc 2100 agagccctct ttgtggcttc cccacgtttg gccttctggg attcactgtg agtgtcctga 2160 gctctcgggg ttgatggttt ttctctcagc atgtctcctc caccacggga ccccagccct 2220 gaccaaccca tggttgcctc atcagcagga aggtgccctt cctggaggat ggtcgccaca 2280 ggcacataat tcaacagtgt ggaagcttta ggggaacatg gagaaagaag gagaccacat 2340 accccaaagt gacctaagaa cactttaaaa agcaacatgt aaatgattgg aaattaatat 2400 agtacagaat atatttttcc cttgttgaga tcttcttttg taatgttttt catgttactg 2460 cctagggcgg tgctgagcac acagcaagtt taataaactt gactgaattc aaaaaaaaaa 2520 <210> SEQ ID NO 84 <211> LENGTH: 366 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 84 Met Ala Leu Pro Pro Gly Pro Ala Ala Leu Arg His Thr Leu Leu Leu 1 5 10 15 Leu Pro Ala Leu Leu Ser Ser Gly Trp Gly Glu Leu Glu Pro Gln Ile 20 25 30 Asp Gly Gln Thr Trp Ala Glu Arg Ala Leu Arg Glu Asn Glu Arg His 35 40 45 Ala Phe Thr Cys Arg Val Ala Gly Gly Pro Gly Thr Pro Arg Leu Ala 50 55 60 Trp Tyr Leu Asp Gly Gln Leu Gln Glu Ala Ser Thr Ser Arg Leu Leu 65 70 75 80 Ser Val Gly Gly Glu Ala Phe Ser Gly Gly Thr Ser Thr Phe Thr Val 85 90 95 Thr Ala His Arg Ala Gln His Glu Leu Asn Cys Ser Leu Gln Asp Pro 100 105 110 Arg Ser Gly Arg Ser Ala Asn Ala Ser Val Ile Leu Asn Val Gln Phe 115 120 125 Lys Pro Glu Ile Ala Gln Val Gly Ala Lys Tyr Gln Glu Ala Gln Gly 130 135 140 Pro Gly Leu Leu Val Val Leu Phe Ala Leu Val Arg Ala Asn Pro Pro 145 150 155 160 Ala Asn Val Thr Trp Ile Asp Gln Asp Gly Pro Val Thr Val Asn Thr 165 170 175 Ser Asp Phe Leu Val Leu Asp Ala Gln Asn Tyr Pro Trp Leu Thr Asn 180 185 190 His Thr Val Gln Leu Gln Leu Arg Ser Leu Ala His Asn Leu Ser Val 195 200 205 Val Ala Thr Asn Asp Val Gly Val Thr Ser Ala Ser Leu Pro Ala Pro 210 215 220 Gly Leu Leu Ala Thr Arg Val Glu Val Pro Leu Leu Gly Ile Val Val 225 230 235 240 Ala Ala Gly Leu Ala Leu Gly Thr Leu Val Gly Phe Ser Thr Leu Val 245 250 255 Ala Cys Leu Val Cys Arg Lys Glu Lys Lys Thr Lys Gly Pro Ser Arg 260 265 270 His Pro Ser Leu Ile Ser Ser Asp Ser Asn Asn Leu Lys Leu Asn Asn 275 280 285 Val Arg Leu Pro Arg Glu Asn Met Ser Leu Pro Ser Asn Leu Gln Leu 290 295 300 Asn Asp Leu Thr Pro Asp Ser Arg Ala Val Lys Pro Ala Asp Arg Gln 305 310 315 320 Met Ala Gln Asn Asn Ser Arg Pro Glu Leu Leu Asp Pro Glu Pro Gly 325 330 335 Gly Leu Leu Thr Ser Gln Gly Phe Ile Arg Leu Pro Val Leu Gly Tyr 340 345 350 Ile Tyr Arg Val Ser Ser Val Ser Ser Asp Glu Ile Trp Leu 355 360 365 <210> SEQ ID NO 85 <211> LENGTH: 1692 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1317) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1394) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1424) <400> SEQUENCE: 85 ctatgtatca tactgagtgt tctgagctgt tagtttcttt ggtgttcatc tagatggaag 60 ctggggcttc cttcctttca gatattggtg ctaacatgaa gctgaccaaa gaattgatgg 120 gatctgcaca ctgtaaagcc ggtttcagga tggctgagct gacggtcaag aaagaagaga 180 agatatgagc cgcctgcatt ttggggtggt ggcagtgaaa tttagacttg tgatttggta 240 tgacaatata tggctttttg tgattgttaa cattaatgaa aacaagaaaa attagttgct 300 caaaagttga aaaatggatt cataaacttt ttattagaat aaggcaaaag aacatattaa 360 aatagaggta aattagaaat gtcaataaga acccatggac attttttata aggagacttt 420 atctgttctg tccctacagt gatttatgct cttggatatt tttgctgtca tcctgacaaa 480 ttctagttgg aatatggaac aagcttattt gtagacctag tgcctgtggc ttctaaagca 540 attttctgaa aagagaaacc actgcctgtt ggaagaatag ttgattccat acctcaagct 600 agggaaaaaa aaaatcagaa ttagtctgtg aattctagat gttgagagaa agcagggttt 660 cattagggca tcggagagtc acaagtccat aggatgcaaa aaggaagatg aaataaaatt 720 gcctgaaaaa cgcacctgaa tttctggcat tgtttactga aaaggctgtg tattgatgaa 780 ccccaattat gtgaggtcta catttaagag tttataatca acagtttgaa aatgcagggt 840 gttgtttctt tctataagga gacaaaacag tcagaaggga gtgtcacagg acattatcac 900 aaaatcaaag ttcttcatga aatgtgttca tttgctagaa ataatgcagc ctattggaga 960 gaatcagggc ttctagtgat gctagggatg accttaagca ttgtttgtaa atcacacttt 1020 ttcctagtct ttcagcagca gctgcacaga gtaggcctgc ttcttcccat gaaagccaca 1080 ctgagtttat caactagtag tgtgtggcac tattgcaagt tatgttgtgt tgttatggcc 1140 atttatccaa cagtgctttc ctctgtgtgg ggctctgcag cctcgttcta tgttattttt 1200 attaccacgt gtctgtgcgc ctcaggtggc aaagcagaat cagcttctct accctcagca 1260 gggctcacta tgactcacta taagggaaga aaatcttaca gatgtcagaa aatgttnggt 1320 aagtggacag tgataaacac aaaacagcaa gtggtcagta tcaaagagaa aaacagtatg 1380 ttggtgaggg agangtgtca aagctggtta aaaaggtgac gggngaaatg taaggggaca 1440 atactccaca aaaatttaga ttgtaactga gcttcttctc ctaaagagat ttaaaaataa 1500 agtataggaa atacatgaag aaacaaagta aaatgccaag gtgtaagttt gaccatgaat 1560 gtctagggaa aaacatactt gcactaaaac aaccaaatat gcaaaaatca agtggaaaaa 1620 caggtcaaaa taatgccagt tgatgtctgt aagaactaaa tgtataataa aatgagcaaa 1680 aaaaaaaaaa aa 1692 <210> SEQ ID NO 86 <211> LENGTH: 195 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (162) <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (188) <400> SEQUENCE: 86 Met Gln Gly Val Val Ser Phe Tyr Lys Glu Thr Lys Gln Ser Glu Gly 1 5 10 15 Ser Val Thr Gly His Tyr His Lys Ile Lys Val Leu His Glu Met Cys 20 25 30 Ser Phe Ala Arg Asn Asn Ala Ala Tyr Trp Arg Glu Ser Gly Leu Leu 35 40 45 Val Met Leu Gly Met Thr Leu Ser Ile Val Cys Lys Ser His Phe Phe 50 55 60 Leu Val Phe Gln Gln Gln Leu His Arg Val Gly Leu Leu Leu Pro Met 65 70 75 80 Lys Ala Thr Leu Ser Leu Ser Thr Ser Ser Val Trp His Tyr Cys Lys 85 90 95 Leu Cys Cys Val Val Met Ala Ile Tyr Pro Thr Val Leu Ser Ser Val 100 105 110 Trp Gly Ser Ala Ala Ser Phe Tyr Val Ile Phe Ile Thr Thr Cys Leu 115 120 125 Cys Ala Ser Gly Gly Lys Ala Glu Ser Ala Ser Leu Pro Ser Ala Gly 130 135 140 Leu Thr Met Thr His Tyr Lys Gly Arg Lys Ser Tyr Arg Cys Gln Lys 145 150 155 160 Met Xaa Gly Lys Trp Thr Val Ile Asn Thr Lys Gln Gln Val Val Ser 165 170 175 Ile Lys Glu Lys Asn Ser Met Leu Val Arg Glu Xaa Cys Gln Ser Trp 180 185 190 Leu Lys Arg 195 <210> SEQ ID NO 87 <211> LENGTH: 802 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 87 ggcattcttg ccgctggccc agtcactatg tagtggaggg gcagacaccc tcccgcaaat 60 tctggaaggt tcttagtctc gactagggca gtagccccag gactcctagt cgccggcttc 120 aggtcactgc cggctgaacg gagctgccgt cgccatgttt ggctgcttgg tggcggggag 180 gctggtgcaa acagctgcac agcaagtggc agaggataaa tttgtttttg acttacctga 240 ttatgaaagt atcaaccatg ttgtggtttt tatgctggga acaatcccat ttcctgaggg 300 aatgggagga tctgtctact tttcttatcc tgattcaaat ggaatgccag tatggcaact 360 cctaggattt gtcacgaatg ggaagccaag tgccatcttc aaaatttcag gtcttaaatc 420 tggagaagga agccaacatc cttttggagc catgaatatt gtccgaactc catctgttgc 480 tcagattgga atttcagtgg aattattaga cagtatggct cagcagactc ctgtaggtaa 540 tgctgctgta tcctcagttg actcattcac tcagttcaca caaaaggtgt tggacaattt 600 ctacaatttt gcttcatcat ttgctgtctc tcaggccccg atgacaccca gcccctctga 660 aatgttcatt ccggccaatg tggttctgaa atggtatgaa aactttcaag ggcgactggc 720 accgaaccct ctcttttggg aaacataatt tgaataaaat aatttttttt ggaaaaaaaa 780 aaaaaaaaaa aaaaaaaaaa aa 802 <210> SEQ ID NO 88 <211> LENGTH: 197 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 88 Met Phe Gly Cys Leu Val Ala Gly Arg Leu Val Gln Thr Ala Ala Gln 1 5 10 15 Gln Val Ala Glu Asp Lys Phe Val Phe Asp Leu Pro Asp Tyr Glu Ser 20 25 30 Ile Asn His Val Val Val Phe Met Leu Gly Thr Ile Pro Phe Pro Glu 35 40 45 Gly Met Gly Gly Ser Val Tyr Phe Ser Tyr Pro Asp Ser Asn Gly Met 50 55 60 Pro Val Trp Gln Leu Leu Gly Phe Val Thr Asn Gly Lys Pro Ser Ala 65 70 75 80 Ile Phe Lys Ile Ser Gly Leu Lys Ser Gly Glu Gly Ser Gln His Pro 85 90 95 Phe Gly Ala Met Asn Ile Val Arg Thr Pro Ser Val Ala Gln Ile Gly 100 105 110 Ile Ser Val Glu Leu Leu Asp Ser Met Ala Gln Gln Thr Pro Val Gly 115 120 125 Asn Ala Ala Val Ser Ser Val Asp Ser Phe Thr Gln Phe Thr Gln Lys 130 135 140 Val Leu Asp Asn Phe Tyr Asn Phe Ala Ser Ser Phe Ala Val Ser Gln 145 150 155 160 Ala Pro Met Thr Pro Ser Pro Ser Glu Met Phe Ile Pro Ala Asn Val 165 170 175 Val Leu Lys Trp Tyr Glu Asn Phe Gln Gly Arg Leu Ala Pro Asn Pro 180 185 190 Leu Phe Trp Glu Thr 195 <210> SEQ ID NO 89 <211> LENGTH: 732 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 89 ctggttttct ccgcgggcgc ctcgggcgga acctggagat aatgggcagc acctggggga 60 gccctggctg ggtgcgactc gctctttgcc tgacgggctt agtgctctcg ctctacgcgc 120 tgcacgtgaa ggcggcgcgc gcccgggacc gggattaccg cgcgctctgc gacgtgggca 180 ccgccatcag ctgttcgcgc gtcttctcct ccaggttgcc tgcggacacg ctgggcctct 240 gtcctgatgc tgctgagctc cctggtgtct ctcgctggtt ctgtctacct ggcctggatc 300 ctgttcttcg tgctctatga tttctgcatt gtttgtatca ccacctatgc tatcaacgtg 360 agcctgatgt ggctcagttt ccggaaggtc caagaacccc agggcaaggc taagaggcac 420 tgagccctca acccaagcca ggctgacctc atctgctttg ctttggcatg tgagccttgc 480 ctaagggggc atatctgggt ccctagaagg ccctagatgt ggggcttcta gattaccccc 540 tcctcctgcc atacccacac atgacaatgg accaaatgtg ccacacgctc gctctttttt 600 acacccagtg cctctgactc tgtccccatg ggctggtctc caaagctctt tccattgccc 660 agggagggaa ggttctgagc aataaagttt cttagatcaa ccaaaaaaaa aaaaaaaaaa 720 aaaaaaaaaa aa 732 <210> SEQ ID NO 90 <211> LENGTH: 92 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 90 Met Gly Ser Thr Trp Gly Ser Pro Gly Trp Val Arg Leu Ala Leu Cys 1 5 10 15 Leu Thr Gly Leu Val Leu Ser Leu Tyr Ala Leu His Val Lys Ala Ala 20 25 30 Arg Ala Arg Asp Arg Asp Tyr Arg Ala Leu Cys Asp Val Gly Thr Ala 35 40 45 Ile Ser Cys Ser Arg Val Phe Ser Ser Arg Leu Pro Ala Asp Thr Leu 50 55 60 Gly Leu Cys Pro Asp Ala Ala Glu Leu Pro Gly Val Ser Arg Trp Phe 65 70 75 80 Cys Leu Pro Gly Leu Asp Pro Val Leu Arg Ala Leu 85 90 <210> SEQ ID NO 91 <211> LENGTH: 901 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 91 ggcgcgatga ggttccggtt ctgtggtgat ctggactgtc ccgactgggt cctggcagaa 60 atcagcacgc tggccaagat gtcctctgtg aagttgcggc tgctctgcag ccaggtacta 120 aaggagctgc tgggacaggg gattgattat gagaagatcc tgaagctcac ggctgacgcc 180 aagtttgagt caggcgatgt gaaggccaca gtggcagtgc tgagtttcat cctctccagt 240 gcggccaagc acagtgtcga tggcgaatcc ttgtccagtg aactgcagca gctggggctg 300 cccaaagagc acgcggccag cctgtgccgc tgttatgagg agaagcaaag ccccttgcag 360 aagcacttgc gggtctgcag cctacgcatg aataggttgg caggtgtggg ctggcgggtg 420 gactacaccc tgagctccag cctgctgcaa tccgtggaag agcccatggt gcacctgcgg 480 ctggaggtgg cagctgcccc agggacccca gcccagcctg ttgccatgtc cctctcagca 540 gacaagttcc aggtcctcct ggcagaactg aagcaggccc agaccctgat gagctccctg 600 ggctgaggag aagggtgttc caggcctgtg tggagccgcc ctgcccgtat ggagtcacgc 660 cctctgaact gctcttcggg aggcagccct ggttctagga tgctgaggcc ctggcccgga 720 ctctggcctc ccagatcccc agctgcctca cttctctctt gagaacttgg ctcagggctc 780 ctgaggacct ttcccagcat taccttccct tcccttgaaa ggcaattgtt ggctgttttc 840 ataagcagga aaaataaaca gaagtataaa ggaaaaaaaa aaaaaaaaaa aaaaaaaaaa 900 a 901 <210> SEQ ID NO 92 <211> LENGTH: 199 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 92 Met Arg Phe Arg Phe Cys Gly Asp Leu Asp Cys Pro Asp Trp Val Leu 1 5 10 15 Ala Glu Ile Ser Thr Leu Ala Lys Met Ser Ser Val Lys Leu Arg Leu 20 25 30 Leu Cys Ser Gln Val Leu Lys Glu Leu Leu Gly Gln Gly Ile Asp Tyr 35 40 45 Glu Lys Ile Leu Lys Leu Thr Ala Asp Ala Lys Phe Glu Ser Gly Asp 50 55 60 Val Lys Ala Thr Val Ala Val Leu Ser Phe Ile Leu Ser Ser Ala Ala 65 70 75 80 Lys His Ser Val Asp Gly Glu Ser Leu Ser Ser Glu Leu Gln Gln Leu 85 90 95 Gly Leu Pro Lys Glu His Ala Ala Ser Leu Cys Arg Cys Tyr Glu Glu 100 105 110 Lys Gln Ser Pro Leu Gln Lys His Leu Arg Val Cys Ser Leu Arg Met 115 120 125 Asn Arg Leu Ala Gly Val Gly Trp Arg Val Asp Tyr Thr Leu Ser Ser 130 135 140 Ser Leu Leu Gln Ser Val Glu Glu Pro Met Val His Leu Arg Leu Glu 145 150 155 160 Val Ala Ala Ala Pro Gly Thr Pro Ala Gln Pro Val Ala Met Ser Leu 165 170 175 Ser Ala Asp Lys Phe Gln Val Leu Leu Ala Glu Leu Lys Gln Ala Gln 180 185 190 Thr Leu Met Ser Ser Leu Gly 195 <210> SEQ ID NO 93 <211> LENGTH: 1579 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 93 gattaaaata ttattttaaa gaaaccactg tttcccccta aaatgtcata agagcactga 60 agaacttgaa atattttttt cagagtttct cacacacttt aaaagtctaa cttttttgtg 120 tgtaagcatt tagcttgcca gcatatttct ttttggctcc ttaaattgcg gttgtgtttg 180 cagtattgtc acttttgctc tcactgttat gttgaataat aattagcata taattgtcta 240 cagaagcaag agcaatctgg aaggaacaaa aatgttttct gtgattaaca gtgaagacct 300 tgtaaatgca gatgtgtgat aaagcattta gtcagtcccc caaacagtca tgccaactgt 360 gaaggaatgt cccacaaaac atttccattc cctgaggaaa aacattttct ttcctacatg 420 tatctctggt atttagaatt gtcactaata accttttcaa gtgattttgg ctattctcta 480 atgaagatat ggtcatttgt ttttcttcct gcaatgtggt gtgcagagat gctgcatatc 540 ctttttatgg gattgcgtgt gaatttgaac catgagacat tcctaataat ttgttgtgag 600 atataccaag catggatgat aagtgtgttt ttagtggtgt gttgtttttt taaagaggtg 660 attcaagtac cgttgctaag ctgtcaacat accaagctgt tgaaaaaatt gaccatttct 720 ttcagaagta attctcagcc tgtggaataa tagcaggtga agacttcata gaaggcgaca 780 gattgatagg gaggctattg aagcagtttt tctgaagcct gcattttgag ttagtttata 840 gtgctaatag attctatata actgtgagag tttggtagta aaccagtagg gattgttttc 900 tctcctaaaa atttgcacac tacttcattg tctacaactt tttacatatt ggaaaataga 960 aattgcaaat acatacatgt atggaaacat attcagattg ggaaaaacat ggacattagt 1020 tttttaaaag ttacgtggag caagatttct atattttgtt ttttaaagga cgcagtcatt 1080 ctttctacta aatccatttc aggctagttc tctgaaaatt ttgccattta tctacagaaa 1140 tttgattata aatatgttcc ttttcaaaga aactttattc tagaacaaaa tagtctatat 1200 ggtacttgat ctacatataa gtggaaaaat tagcagtatt tgaaagctca gtttatgtca 1260 ttgtcttaac ttcagataca aataactgaa cagaaagtta taacctttaa tatctcatgt 1320 tctgtttttt attcagtatt ttcctatatg ttaattcaat tatatacttc tgaatggcac 1380 cttacttttt ggaaacaaat cttctgttat ttacaaaata tataattttt aaaaaacatt 1440 taaaaaaatc caaagctgct ctcgataata gtcaacattt gcatatatat ggaatttctt 1500 actttttttc tcccaaactc tatttaataa acttatttta atgtttgtat aaaaaaaaaa 1560 aaaaaaaaaa aaaaaaaaa 1579 <210> SEQ ID NO 94 <211> LENGTH: 127 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 94 Met Ser His Lys Thr Phe Pro Phe Pro Glu Glu Lys His Phe Leu Ser 1 5 10 15 Tyr Met Tyr Leu Trp Tyr Leu Glu Leu Ser Leu Ile Thr Phe Ser Ser 20 25 30 Asp Phe Gly Tyr Ser Leu Met Lys Ile Trp Ser Phe Val Phe Leu Pro 35 40 45 Ala Met Trp Cys Ala Glu Met Leu His Ile Leu Phe Met Gly Leu Arg 50 55 60 Val Asn Leu Asn His Glu Thr Phe Leu Ile Ile Cys Cys Glu Ile Tyr 65 70 75 80 Gln Ala Trp Met Ile Ser Val Phe Leu Val Val Cys Cys Phe Phe Lys 85 90 95 Glu Val Ile Gln Val Pro Leu Leu Ser Cys Gln His Thr Lys Leu Leu 100 105 110 Lys Lys Leu Thr Ile Ser Phe Arg Ser Asn Ser Gln Pro Val Glu 115 120 125 <210> SEQ ID NO 95 <211> LENGTH: 1891 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 95 agctggaggg agtcatggtg tcactggggt acaggagggt gaatgaaggg catgcaggcc 60 ctcagcccgg gctgtgccag ccctcccagc cccaggccca tctgagggac caagacgctg 120 ttacgcaggc ccttctttcc agctatcagc actttcagca tcggctcttc agcagatcca 180 aaccccctca gcaacttgca gaggacctgt cccctctcaa aagtcccctg gcctagggtg 240 gggaccccca aacctacggc aaagccagca acagtagcag cctgctccca tttgctgggg 300 aggagatcat cttgttcccc tggcccccca ctctccctcc atgtccatcc aaaaaccata 360 aaatcactgg gttccacatc agcctccatg aggccaagcc ttgtacctgc aaggctcttg 420 gcctaaccat tcctctgtcc tcttctctgg cctgcctggg gagcccgtga aggccgcacg 480 ggtgcctcca gcctgagaca tcaggggaga gcctgcagct gagttcagca gaaaggagga 540 atcctggccc tcaggaagaa gatagtcaca tgtttttctt ccttgtcccc acagccccca 600 gaacaacatt ctccctgctg gcagcccttc catgtctcca aacctgggtc agagtgaaag 660 gacctttggg ggtgggtggg agcaaagggc ccacctgctg gttggtgaaa gcagtggtgc 720 cggagtgcta ggtaccgcac gagagggtgc gggggcttgg gaagcagacc agggttggac 780 aaaaccccat gagggcgggg agctggaaga aaagtctctt ggggacctct ggggcaagga 840 gctgagaagt cctgcagcac caggtgaaac ttgcttacag tggatgccac ttttaggcct 900 ctggaccgca gatgccttct tccttctgga cacctggctt ctgggcctcc aggtaaagag 960 agagagccag ccaagcctgt tcccctcagt cctcctttgc tcctgctgct tcttccaaca 1020 gccactgtta ggaggtagta gaccccagcc tcaaggctct gaccttcttc atgtgggcac 1080 agaggtcctg acactctggc agggcctgag ctggggcagg cctccctcag ggccaggggc 1140 gatggcaccc cggggacagg cagacctcct tcctgccgtc agcaccccct tccttatcac 1200 tgtctggtct ccgagcttcg gctgcagcct gaggtgtgtc ctgggctcct cagagcctga 1260 agcaagcttt tggaagcctg cagtcctccc agctccagtg cagaagcctc tctctccagc 1320 ctttccccag gcaggagttg gggttggggg cctctgtccc tcatcgctta ccttggaaag 1380 gtgggaagct ggcaatctgc accttggggc ctgggctccc cctctctgtg ccagcggctt 1440 cccagcacct gggaggggct gcagccccag ctggactcca gcctgtccct cttagcactc 1500 tagctgccca ctccagggca gggactcgaa accccctccg tcctgagcag ccacctccag 1560 ggccctgttt gggaccactc tctcagtccc caggtcctca gggccccaga gcgggagggt 1620 ctcctacctg gaagtccccc tgagctccag ggcccagccc tacctgccag tgctggtgtc 1680 agggcactca accccgagtg tggggccacg ccccttgcca tgcccacggc ctcctcctgt 1740 agcccctgcc tgcccccccg atgctgcacg ggcccgccct ggtggggctc ggcgagtaat 1800 gtgttttgtc cccagttaac caccattctg cggcctggtt ctgcaaggaa ccagggctgc 1860 cccaccacca cgaaacacaa aaaaaaaaaa a 1891 <210> SEQ ID NO 96 <211> LENGTH: 287 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 96 Met Ser Pro Asn Leu Gly Gln Ser Glu Arg Thr Phe Gly Gly Gly Trp 1 5 10 15 Glu Gln Arg Ala His Leu Leu Val Gly Glu Ser Ser Gly Ala Gly Val 20 25 30 Leu Gly Thr Ala Arg Glu Gly Ala Gly Ala Trp Glu Ala Asp Gln Gly 35 40 45 Trp Thr Lys Pro His Glu Gly Gly Glu Leu Glu Glu Lys Ser Leu Gly 50 55 60 Asp Leu Trp Gly Lys Glu Leu Arg Ser Pro Ala Ala Pro Gly Glu Thr 65 70 75 80 Cys Leu Gln Trp Met Pro Leu Leu Gly Leu Trp Thr Ala Asp Ala Phe 85 90 95 Phe Leu Leu Asp Thr Trp Leu Leu Gly Leu Gln Val Lys Arg Glu Ser 100 105 110 Gln Pro Ser Leu Phe Pro Ser Val Leu Leu Cys Ser Cys Cys Phe Phe 115 120 125 Gln Gln Pro Leu Leu Gly Gly Ser Arg Pro Gln Pro Gln Gly Ser Asp 130 135 140 Leu Leu His Val Gly Thr Glu Val Leu Thr Leu Trp Gln Gly Leu Ser 145 150 155 160 Trp Gly Arg Pro Pro Ser Gly Pro Gly Ala Met Ala Pro Arg Gly Gln 165 170 175 Ala Asp Leu Leu Pro Ala Val Ser Thr Pro Phe Leu Ile Thr Val Trp 180 185 190 Ser Pro Ser Phe Gly Cys Ser Leu Arg Cys Val Leu Gly Ser Ser Glu 195 200 205 Pro Glu Ala Ser Phe Trp Lys Pro Ala Val Leu Pro Ala Pro Val Gln 210 215 220 Lys Pro Leu Ser Pro Ala Phe Pro Gln Ala Gly Val Gly Val Gly Gly 225 230 235 240 Leu Cys Pro Ser Ser Leu Thr Leu Glu Arg Trp Glu Ala Gly Asn Leu 245 250 255 His Leu Gly Ala Trp Ala Pro Pro Leu Cys Ala Ser Gly Phe Pro Ala 260 265 270 Pro Gly Arg Gly Cys Ser Pro Ser Trp Thr Pro Ala Cys Pro Ser 275 280 285 <210> SEQ ID NO 97 <211> LENGTH: 2192 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (891) <400> SEQUENCE: 97 ctgttaacag tactttaatt gagccgtctg tgttctagtt ctgtccagag cccccgccgt 60 tttcccctcc agcacaggat tcatttcagg atcatcactt gcgttatatg cccaaggggt 120 ccctctcttg gtgtgtgggc agagccagag ctgggaacaa tgggggtggt gtgtgggttc 180 tgggctcagg cttcctggat ttggcattgg cctcctgatg tcatgtatcg gctggaagac 240 tcaggacaac cttctgcctt tctgagcctc cgtttcctca aacctgaagt gaggatgaag 300 gcagcgtgca tggcttaggg gcgttgggtg ctcagcatcg tgcgtgagat gctgagtgtt 360 caccactcag tattagccat ggatgtcttt ttggaaattc cccacagccc tctccacaca 420 gagtcaaatg tcaaaaacct gctgccaact ggcacctggt tctcacagct gctctctggg 480 gctctggggc ctgtcagagc cacctgtcca agattcagga ttcagcacat cacctctgcc 540 ccacccctac cggcagcatt cctttcctac ctgtccagcc tcttctctgt ccccagccac 600 attccccact cctgccccca aactcttggc ctagaaggcc ctggcctgct ccccaggcct 660 cctctgctaa gccttgccta cctgtcccca ctgtgccccc cactgcctgc gcatctctgg 720 ccagcacagg cgtgggagga actatggctc ttcttcctta ggaagagtct ctgacaagta 780 ggactttgtt ttcttcccag catgcactgc agtgcaggtg tcttaaccct tggcgcacac 840 acaggatgaa ggcagagagc caactattga gggtgggaat tgggaagcct nctgcctgga 900 tcatcttaga aactggaggc cccttttcac tcgggtctcc cctgtgccgt gcacgccacc 960 tctttcaggg cccactcacc ctgggtggaa ttggatggcc actttgccag aacttcttcg 1020 tcttttgttg acctgttctg gccattaaga ccaccttctc ttttctgggg ggtttccgcc 1080 tgtcctttgc tacggtactt ggagacaggt gagctcactt tgttctttgc tttaagtctg 1140 ttacctcttg agccaaggtg aggcacctcc aggggcagcc aggcccctgc ttctggcccc 1200 gcacaccctc tacactttga cctttccggc tgtttacctg cctggagtgt gcctcactcc 1260 cctcccctca gttgatcttt tactgtgctc tctctatgta gcgccctctt gctcccttct 1320 aaaactccat tctggaaaaa ctcagccatt gtcttttttt gtttgttttt ttcctgtttt 1380 aatctttagt gagcctgtgt atccataggg cttgtgagga aaaacagcgg ccctttgccc 1440 caaccagcat ccaccctagg gacaatcact ttcaactcag tggactcttg gaatttgcgc 1500 ccgtagctct aaaaactgtg ctggctgctt ctcagtcttt cagctcaggg cagaatccat 1560 tgccttccac caggagagct gaacatcagt gctctcgtgg ctccatgagt cctcttagcc 1620 cctttctctc ctctcatctt ccctggtagt tccccataat tgtgatgaga atacctgtgt 1680 aggtcagtca tcggagtggt gtgaagggat gtgtggccca gtgacatctc agctgccatt 1740 tctgcttgct ttgccgtgag tgttctttgc tttgtttctt ggctctaacc caattccagg 1800 cttcctcctg attgtttcac tcttctctct ggccacttat ttatttattt ttcgagatgg 1860 agtctccctc tgtcacccag gctggagtgc attggtgtgt tctctgctca ctgcaacctc 1920 tgcctcctgg gttcaagcaa ttctcctacc tcagcctcct gagtagctgg gactacaggc 1980 gtgtgccact atgcctggct aatttattta tttttatttt tttatttttt tgagatggag 2040 tctcactctg tcacccaggc tggagtgcag tggcgcgttc tcggctcact gcaactccgc 2100 ctcccaggtt cacgccattc tcctacctca gcctcccagg tagctgggac tacaggtgct 2160 cgccaccacc acgaaacaaa aaaaaaaaaa aa 2192 <210> SEQ ID NO 98 <211> LENGTH: 141 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 98 Met Leu Ser Val His His Ser Val Leu Ala Met Asp Val Phe Leu Glu 1 5 10 15 Ile Pro His Ser Pro Leu His Thr Glu Ser Asn Val Lys Asn Leu Leu 20 25 30 Pro Thr Gly Thr Trp Phe Ser Gln Leu Leu Ser Gly Ala Leu Gly Pro 35 40 45 Val Arg Ala Thr Cys Pro Arg Phe Arg Ile Gln His Ile Thr Ser Ala 50 55 60 Pro Pro Leu Pro Ala Ala Phe Leu Ser Tyr Leu Ser Ser Leu Phe Ser 65 70 75 80 Val Pro Ser His Ile Pro His Ser Cys Pro Gln Thr Leu Gly Leu Glu 85 90 95 Gly Pro Gly Leu Leu Pro Arg Pro Pro Leu Leu Ser Leu Ala Tyr Leu 100 105 110 Ser Pro Leu Cys Pro Pro Leu Pro Ala His Leu Trp Pro Ala Gln Ala 115 120 125 Trp Glu Glu Leu Trp Leu Phe Phe Leu Arg Lys Ser Leu 130 135 140 <210> SEQ ID NO 99 <211> LENGTH: 1774 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 99 cagaggagga ataatgagga actggtagtg tcagcctcct gtaaggaacc agagcaggag 60 ccagtgccag cacagttcca gaaagtaaag cccccaaaga ctaatcataa acgaggaagg 120 aaataggcag tcagtgtaaa agtgctccta ggaaagcaga tgtgatgctg ttgtcacggg 180 gacctgtgct gggaggactg agtgaagatt ctttcagctg tttgtgtaag gctgtgactt 240 tctcagctcc ttcctcctgt gtaaatttca ctgtcttccc ttcttacatt ttgattcccc 300 cctccccttt tagtaggttt tcctgctatt cctcgtcaag tcctcttgtt tttttatctt 360 gcccaaagag ctccctctca aggccaacta taggctccgc ttgccctgta caaaactaag 420 aaacctcttt ggttgtcctt tccttcctgg ggtatagaat gttcttggaa gctccattga 480 tttagtagct gctccatcat ctagcttgtg aaaccattcc aaactaattt tttaaaacca 540 taactgattt gtcattttgt atttgtgata taacaagtct agaagttaga actgttgtca 600 ttcacataat aagattactc tgtctccttg ggaaaaaaac tttatggagg ctgtttgtcc 660 tctcaatatg gttttaagat tgaaagtaag aaaacggatt taggatgaaa actctagaac 720 taccctatgc tgtttatact gggaaatgct ttgtaccaag tagcagtgac tagacccaca 780 gacatgaaaa gcaaccttag gagtaaagtg acccaaacat taaaatgaca ggaaagagaa 840 agtagaagca gcaataaata ctgccccaac ttccttggag cccgaggcct catccatagc 900 tatgatcact tgccctctga agcttatttt tgcttctttg gttttaagaa ttgagaaata 960 tcacattgcc cctgatgttt tgaacagtct ccaagtgctc ctggtagtgc cactaaggga 1020 aaaccaaggt gcgcattcct tctccctgga ctttacctta cttgttagtc tacgccccac 1080 tgtttccacc catcccctta gccaacctct gtctttttga attttctgag aatattgtcc 1140 tatcctcttt tatatatgga gttctctcct ctttatatcc tgagactttg acaccagatg 1200 tagatattta tctggagctg gaaagaaaaa ttctttttct gtacctcatg cctatctggt 1260 aatgtttaat gggttatttc tctttgaggg tggctttctc tggaacattg gttagagcag 1320 ctttgttgtc gtgtttctgg attctcttcc ccattttgcg taaatattgg tcttatatat 1380 tcttgcctat tttgtggcat atgccacata aaaaatgaac ctgatataga caagtactac 1440 cttttcaaat tctgaaaggc tattaccact ttaactcttt gtgctcctcc aaatagcttt 1500 aaaatgtggg cttttgtgaa gaccactttc aaacaaggga gcactgaaac ctgaattgga 1560 tactgccaga ataggtagtt ttgaaacaag ttaaggacat ggtatatgca ctctgcattt 1620 tcattggcag tgtgccctta aagccctttc agtagatgag ggttgtcagg gaggagaaat 1680 gaagaagcta tgttaatttc tggtgagtaa gacctgggga atgtttggca atgacaaaag 1740 aaataaatga ctctcaggaa aaaaaaaaaa aaaa 1774 <210> SEQ ID NO 100 <211> LENGTH: 84 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 100 Met Leu Leu Ser Arg Gly Pro Val Leu Gly Gly Leu Ser Glu Asp Ser 1 5 10 15 Phe Ser Cys Leu Cys Lys Ala Val Thr Phe Ser Ala Pro Ser Ser Cys 20 25 30 Val Asn Phe Thr Val Phe Pro Ser Tyr Ile Leu Ile Pro Pro Ser Pro 35 40 45 Phe Ser Arg Phe Ser Cys Tyr Ser Ser Ser Ser Pro Leu Val Phe Leu 50 55 60 Ser Cys Pro Lys Ser Ser Leu Ser Arg Pro Thr Ile Gly Ser Ala Cys 65 70 75 80 Pro Val Gln Asn <210> SEQ ID NO 101 <211> LENGTH: 1324 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 101 ggtgtcgagc cctctggcag agggttaacc tgggtcaaat gcacggattc tcacctcgta 60 cagttacgct ctcccgcggc acgtccgcga ggacttgaag tcctgagcgc tcaagtttgt 120 ccgtaggtcg agagaaggcc atggaggtgc cgccaccggc accgcggagc tttctctgta 180 gagcattgtg cctatttccc cgagtctttg ctgccgaagc tgtgactgcc gattcggaag 240 tccttgagga gcgtcagaag cggcttccct acgtcccaga gccctattac ccggaatctg 300 gatgggaccg cctccgggag ctgtttggca aagatgaaca gcagagaatt tcaaaggacc 360 ttgctaatat ctgtaagacg gcagctacag caggcatcat tggctgggtg tatgggggaa 420 taccagcttt tattcatgct aaacaacaat acattgagca gagccaggca gaaatttatc 480 ataaccggtt tgatgctgtg caatctgcac atcgtgctgc cacacgaggc ttcattcgtt 540 atggctggcg ctggggttgg agaactgcag tgtttgtgac tatattcaac acagtgaaca 600 ctagtctgaa tgtataccga aataaagatg ccttaagcca ttttgtaatt gcaggagctg 660 tcacgggaag tctttttagg ataaacgtag gcctgcgtgg cctggtggct ggtggcataa 720 ttggagcctt gctgggcact cctgtaggag gcctgctgat ggcatttcag aagtactctg 780 gtgagactgt tcaggaaaga aaacagaagg atcgaaaggc actccatgag ctaaaactgg 840 aagagtggaa aggcagacta caagttactg agcacctccc tgagaaaatt gaaagtagtt 900 tacaggaaga tgaacctgag aatgatgcta agaaaattga agcactgcta aaccttccta 960 gaaacccttc agtaatagat aaacaagaca aggactgaaa gtgctctgaa cttgaaactc 1020 actggagagc tgaagggagc tgccatgtcc gatgaatgcc aacagacagg ccactctttg 1080 gtcagcctgc tgacaaattt aagtgctggt acctgtggtg gcagtggctt gctcttgtct 1140 ttttcttttc tttttaacta agaatggggc tgttgtactc tcactttact tatccttcaa 1200 tttaaataca tacttatgtt tgtattaatc tatcaatata tgcatacatg aatatatcca 1260 cccacctaga ttttaagcag taaataaaac atttcgcaaa agaaaaaaaa aaaaaaaaaa 1320 aaaa 1324 <210> SEQ ID NO 102 <211> LENGTH: 285 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 102 Met Glu Val Pro Pro Pro Ala Pro Arg Ser Phe Leu Cys Arg Ala Leu 1 5 10 15 Cys Leu Phe Pro Arg Val Phe Ala Ala Glu Ala Val Thr Ala Asp Ser 20 25 30 Glu Val Leu Glu Glu Arg Gln Lys Arg Leu Pro Tyr Val Pro Glu Pro 35 40 45 Tyr Tyr Pro Glu Ser Gly Trp Asp Arg Leu Arg Glu Leu Phe Gly Lys 50 55 60 Asp Glu Gln Gln Arg Ile Ser Lys Asp Leu Ala Asn Ile Cys Lys Thr 65 70 75 80 Ala Ala Thr Ala Gly Ile Ile Gly Trp Val Tyr Gly Gly Ile Pro Ala 85 90 95 Phe Ile His Ala Lys Gln Gln Tyr Ile Glu Gln Ser Gln Ala Glu Ile 100 105 110 Tyr His Asn Arg Phe Asp Ala Val Gln Ser Ala His Arg Ala Ala Thr 115 120 125 Arg Gly Phe Ile Arg Tyr Gly Trp Arg Trp Gly Trp Arg Thr Ala Val 130 135 140 Phe Val Thr Ile Phe Asn Thr Val Asn Thr Ser Leu Asn Val Tyr Arg 145 150 155 160 Asn Lys Asp Ala Leu Ser His Phe Val Ile Ala Gly Ala Val Thr Gly 165 170 175 Ser Leu Phe Arg Ile Asn Val Gly Leu Arg Gly Leu Val Ala Gly Gly 180 185 190 Ile Ile Gly Ala Leu Leu Gly Thr Pro Val Gly Gly Leu Leu Met Ala 195 200 205 Phe Gln Lys Tyr Ser Gly Glu Thr Val Gln Glu Arg Lys Gln Lys Asp 210 215 220 Arg Lys Ala Leu His Glu Leu Lys Leu Glu Glu Trp Lys Gly Arg Leu 225 230 235 240 Gln Val Thr Glu His Leu Pro Glu Lys Ile Glu Ser Ser Leu Gln Glu 245 250 255 Asp Glu Pro Glu Asn Asp Ala Lys Lys Ile Glu Ala Leu Leu Asn Leu 260 265 270 Pro Arg Asn Pro Ser Val Ile Asp Lys Gln Asp Lys Asp 275 280 285 <210> SEQ ID NO 103 <211> LENGTH: 977 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 103 ggcagaggca tcatggaggg tccccgggga tggctggtgc tctgtgtgct ggccatatcg 60 ctggcctcta tggtgaccga ggacttgtgc cgagcaccag acgggaagaa aggggaggca 120 ggaagacctg gcagacgggg gcggccaggc ctcaaggggg agcaagggga gccgggggcc 180 cctggcatcc ggacaggcat ccaaggcctt aaaggagacc agggggaacc tgggccctct 240 ggaaaccccg gcaaggtggg ctacccaggg cccagcggcc ccctcggagc ccgtggcatc 300 ccgggaatta aaggcaccaa gggcagccca ggaaacatca aggaccagcc gaggccagcc 360 ttcaccgcca ttcggcggaa ccccccaatg gggggcaacg tggtcatctt cgacacggtc 420 atcaccaacc aggaagaacc gtaccagaac cactccggcc gattcgtctg cactgtaccc 480 ggctactact acttcacctt ccaggtgctg tcccagtggg aaatctgcct gtccatcgtc 540 tcctcctcaa ggggccaggt ccgacgctcc ctgggcttct gtgacaccac caacaagggg 600 ctcttccagg tggtgtcagg gggcatggtg cttcagctgc agcagggtga ccaggtctgg 660 gttgaaaaag accccaaaaa gggtcacatt taccagggct ctgaggccga cagcgtcttc 720 agcggcttcc tcatcttccc atctgcctga gccagggaag gaccccctcc cccacccacc 780 tctctggctt ccatgtccgc ctgtaaaatg ggggcgctat tgcttcagct gctgaaggga 840 gggggctggc tctgagagcc ccaggactgg ctgccccgtg acacatgctc taagaagctc 900 gtttcttaga cctcttcctg gaataaacat ctgtgtctgt gtctgccaaa aaaaaaaaaa 960 aaaaaaaaaa aaaaaaa 977 <210> SEQ ID NO 104 <211> LENGTH: 245 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 104 Met Glu Gly Pro Arg Gly Trp Leu Val Leu Cys Val Leu Ala Ile Ser 1 5 10 15 Leu Ala Ser Met Val Thr Glu Asp Leu Cys Arg Ala Pro Asp Gly Lys 20 25 30 Lys Gly Glu Ala Gly Arg Pro Gly Arg Arg Gly Arg Pro Gly Leu Lys 35 40 45 Gly Glu Gln Gly Glu Pro Gly Ala Pro Gly Ile Arg Thr Gly Ile Gln 50 55 60 Gly Leu Lys Gly Asp Gln Gly Glu Pro Gly Pro Ser Gly Asn Pro Gly 65 70 75 80 Lys Val Gly Tyr Pro Gly Pro Ser Gly Pro Leu Gly Ala Arg Gly Ile 85 90 95 Pro Gly Ile Lys Gly Thr Lys Gly Ser Pro Gly Asn Ile Lys Asp Gln 100 105 110 Pro Arg Pro Ala Phe Thr Ala Ile Arg Arg Asn Pro Pro Met Gly Gly 115 120 125 Asn Val Val Ile Phe Asp Thr Val Ile Thr Asn Gln Glu Glu Pro Tyr 130 135 140 Gln Asn His Ser Gly Arg Phe Val Cys Thr Val Pro Gly Tyr Tyr Tyr 145 150 155 160 Phe Thr Phe Gln Val Leu Ser Gln Trp Glu Ile Cys Leu Ser Ile Val 165 170 175 Ser Ser Ser Arg Gly Gln Val Arg Arg Ser Leu Gly Phe Cys Asp Thr 180 185 190 Thr Asn Lys Gly Leu Phe Gln Val Val Ser Gly Gly Met Val Leu Gln 195 200 205 Leu Gln Gln Gly Asp Gln Val Trp Val Glu Lys Asp Pro Lys Lys Gly 210 215 220 His Ile Tyr Gln Gly Ser Glu Ala Asp Ser Val Phe Ser Gly Phe Leu 225 230 235 240 Ile Phe Pro Ser Ala 245 <210> SEQ ID NO 105 <211> LENGTH: 1034 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (618) <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (905..906) <400> SEQUENCE: 105 ctcaggcctt gagggacact tccttcctcc ccactcgcct cctctccact agactttggt 60 tcctagaggg cgtggggccg ggtctgaggt tcttgcctgc cttccctccc attggtcttt 120 ggttgctcat ccctctaact gcaccccttc ttggtccttc ctccacagac ttcagataat 180 agataagtca ttagcaaacc agaccgaatc tttagggtga agagctcccc aaagccatct 240 ggtgaggtca ttttggggac cagggactga ttatttgtca cctggatcac aaagatggga 300 ctgtctgctc aggctggtgg tgacaggatc ctgacccgtg gtcctctccc gctccctctg 360 ctccaccagg acacatgtat aggacactgt gctgtgtgca gtggagaaat ctccctgggc 420 caggggaaag ttcagacagt gcctctagat tgtgttttgc ctcctccaat gttgagttga 480 catctggacc ccagagccca gcagggcttt ctgtcagaca tgctagggtg gtagaaatgg 540 gccctccagg tccccttgca gtgcactggg cagagacctc cggaaagccg gcagcgggag 600 cgctttctgg gccgcttnct cccgcacagt gttcccaacc cagtccatcc ggaaaacagt 660 ctgtacagca aatgctgtgt gagatcttag gcttttcact ttttttgttt tgttttgttt 720 ttgaaagata gaaaaaaata caattaacaa gcctcttttg taaatgggtt tcctttctat 780 gtataaaatc gtggtggtcc cttgttttta catgttcatg ctgtgtaatt ttgagatgtt 840 actgagatat gttctgaaca taatgtgcat ttttttctgt acagatgaaa taggcgaatt 900 taatnnagtg attgatggtt ttttaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 960 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 1020 aaaaaaaaaa aaaa 1034 <210> SEQ ID NO 106 <211> LENGTH: 118 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (82) <400> SEQUENCE: 106 Met Tyr Arg Thr Leu Cys Cys Val Gln Trp Arg Asn Leu Pro Gly Pro 1 5 10 15 Gly Glu Ser Ser Asp Ser Ala Ser Arg Leu Cys Phe Ala Ser Ser Asn 20 25 30 Val Glu Leu Thr Ser Gly Pro Gln Ser Pro Ala Gly Leu Ser Val Arg 35 40 45 His Ala Arg Val Val Glu Met Gly Pro Pro Gly Pro Leu Ala Val His 50 55 60 Trp Ala Glu Thr Ser Gly Lys Pro Ala Ala Gly Ala Leu Ser Gly Pro 65 70 75 80 Leu Xaa Pro Ala Gln Cys Ser Gln Pro Ser Pro Ser Gly Lys Gln Ser 85 90 95 Val Gln Gln Met Leu Cys Glu Ile Leu Gly Phe Ser Leu Phe Leu Phe 100 105 110 Cys Phe Val Phe Glu Arg 115 <210> SEQ ID NO 107 <211> LENGTH: 882 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 107 cccatctgcc cctcacctcg tcatccaggg acccaaaccc tgcaccttcc atgtgggccc 60 acagatcctt ggcaggtacc tgaggtgcac cattgagtgt cggatttggg gttagcatcc 120 agaaagaaga atgcgcatga cgctctgtga aggctggaac tcaggtcttc agggagagaa 180 aggaagactg gattgcacct tgatgcctcc tgaggaggcg gaccccctct tgaggtgggc 240 gtgggcccgg cccagcctta tccaagtcgc tctgtccacc tcccccttcc tggcccccac 300 cccactcctg tgcctcccag gagccctccc tgtgctccac ctgcctccgc agaaggaagc 360 ctctttctct gtttccctgg gtgagggggc tggcaggtgg ctaaccccat ttagcatctc 420 caggccctgc catggtgtct catcttgctg ttatctctag atctttccct cctcccattt 480 cctttagtag ttgaattttg caaagcttgt agcagtagct cagttgcctg cagcatcctt 540 gtgtgtagat aaattagtcg acagaaactc agcactgggg acaggattgc aaagtcgggg 600 acatagatgc agacagttgt tgagatttgg ggatagccgg gcttgtgagc ggtgcccatt 660 tccagatgaa gcctttcagc ccttctgagt ccccggccct tggtgcgatg tctgtgagtt 720 tgacctgccc agcgtgtggg ctggctcaat gctgaataaa gtgggtttgt gtcaaaaaaa 780 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 840 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 882 <210> SEQ ID NO 108 <211> LENGTH: 109 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 108 Met Arg Met Thr Leu Cys Glu Gly Trp Asn Ser Gly Leu Gln Gly Glu 1 5 10 15 Lys Gly Arg Leu Asp Cys Thr Leu Met Pro Pro Glu Glu Ala Asp Pro 20 25 30 Leu Leu Arg Trp Ala Trp Ala Arg Pro Ser Leu Ile Gln Val Ala Leu 35 40 45 Ser Thr Ser Pro Phe Leu Ala Pro Thr Pro Leu Leu Cys Leu Pro Gly 50 55 60 Ala Leu Pro Val Leu His Leu Pro Pro Gln Lys Glu Ala Ser Phe Ser 65 70 75 80 Val Ser Leu Gly Glu Gly Ala Gly Arg Trp Leu Thr Pro Phe Ser Ile 85 90 95 Ser Arg Pro Cys His Gly Val Ser Ser Cys Cys Tyr Leu 100 105 <210> SEQ ID NO 109 <211> LENGTH: 1547 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 109 cctaaaagtc ctgcccttta gttcagtgga ttctggattc tgaggatact cttggtcctt 60 tccagagatg aaggcaggca ggggtcaggg cccacagaag ggaatcccta tattcttggg 120 gttgtctgag ccagggctca tgcctgtctg gtgctttcaa ccaaacctct ctcatgggct 180 ctgtaaaagg aacaatcagg ccattctgaa tcccccagat cttgtaccta ccttttagaa 240 ttgtcttgag agtgtgtgtg ctgattctcc taaagtactt cgtgtggttc ctgacctata 300 ataagtgctt cataaatctt agtcattatt gttaaaatcc caaagagtgg ttttgctcga 360 gtctgaatcc aaaaaggaag ctccaggtaa gaggagaaac tagagaacag gacacagaaa 420 ccatcctgtg ttttttctat cctgtgaaac catcaccatg acactggcct tccctctcag 480 tgtggcctca tcctccatgt ccctccctgt agtcccctta actgtgaagt gtccagcctc 540 tccagcactt actcccaggc ccagctccac ttcaggcagg cctgctgggg ctcagaatag 600 cccagctgct gtctcagcag atggccaggc taattttagc catgtggtac tcacccaggg 660 accaggctgg gctttttaga tttgaataag ccagtgtgca actttggttt agagccaata 720 acaaagtttg gagctgttgt gatctctgtg tctgcctagc actttataag attccagaaa 780 tataatttta aaggattttg tttctgtgaa ccaacaagaa cccaagctat ggagccagca 840 ggcagtcaag ccagcagggt attgatggag ggtggtgaga agcagatggt ggcaccagct 900 cctgcctctt ctccctgatg acaaagcggg tggcagggcc tcagtatccc gggtgcactg 960 tgctctcact gctctcctgg ccaaagtgaa agaaggccgc cgccaactca gcctcctgga 1020 tcatcctctg aaccagtcgt gggtggcagg ctgcatctta atgatgtgga acaaatgtgg 1080 tccgggagaa gtcagcccga tgccagcaag aacctactct ggcactttca tgtgcagtaa 1140 atagagacaa cataatgtga agtaggcaga tgtggaaaaa ggctcagaga ggtaagaggt 1200 cccaagagag gctgagattg agccaggttg agaacgtgtc ttttaaattg tgatgtttct 1260 gccttgttgt tcttcatatg tgaagactgc ctttcatccc agttcttcca gagagttcag 1320 ggacaacaca cagtgactcg gaaagccaca ttccagcctg ccttcacctt tccatgatta 1380 atttctagtt gcagaagcaa gttgcccaga gaagacagta gaatgaggag accggactgg 1440 tcatgcttcc taaactgggt ccatggactc ttaaaagttg gtttgggtgg tctttgggga 1500 atctgtttgt ccgttgcgct gtttccgctt aaaaaaaaaa aaaaaaa 1547 <210> SEQ ID NO 110 <211> LENGTH: 73 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 110 Met Thr Leu Ala Phe Pro Leu Ser Val Ala Ser Ser Ser Met Ser Leu 1 5 10 15 Pro Val Val Pro Leu Thr Val Lys Cys Pro Ala Ser Pro Ala Leu Thr 20 25 30 Pro Arg Pro Ser Ser Thr Ser Gly Arg Pro Ala Gly Ala Gln Asn Ser 35 40 45 Pro Ala Ala Val Ser Ala Asp Gly Gln Ala Asn Phe Ser His Val Val 50 55 60 Leu Thr Gln Gly Pro Gly Trp Ala Phe 65 70 <210> SEQ ID NO 111 <211> LENGTH: 650 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 111 cagaagtagt ctgtctatcc cttttatgaa taaaaaagat attactgaag agaaatacag 60 tatttgtgtc atataatact taagctgaaa aagctaagtc tgaataaatc agtcattggc 120 atttacctta catatggcaa tgaatagtga ctttatagtt agaaatgtat gggtgaaaca 180 gtatcagaat gataatgtag aaacatatat aagccccaga ctgcccccta cagcaaaatg 240 cgattattaa taactattct gcttgaaata tttggtgaga ttctttcacc catcaagtgc 300 ttgtttgtta atattttaat cgggtcggtg tttctttggt tttgtaaatt gtgcacgttt 360 acaaagcact ggctgttctc aggcagtttt caagtttaaa tattcttgcc tttagggtca 420 ttatttgttc ctggttcccc cactctgcca ttactttttc atactttttc cacaaagatt 480 tcagccatac tccctgactt tggtttatct tctactctga catatctgca tgaagtagtt 540 tctgtctgaa atgtcttgaa accagggatg ttcttataat aatacttact gtgcagtgag 600 tggatagcca caagtaatcc ataattttac tttttaaaaa aaaaaaaaaa 650 <210> SEQ ID NO 112 <211> LENGTH: 53 <212> TYPE: PRT <400> SEQUENCE: 112 Met Arg Leu Leu Ile Thr Ile Leu Leu Glu Ile Phe Gly Glu Ile Leu 1 5 10 15 Ser Pro Ile Lys Cys Leu Phe Val Asn Ile Leu Ile Gly Ser Val Phe 20 25 30 Leu Trp Phe Cys Lys Leu Cys Thr Phe Thr Lys His Trp Leu Phe Ser 35 40 45 Gly Ser Phe Gln Val 50 <210> SEQ ID NO 113 <211> LENGTH: 1136 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 113 ggaagatggc gtaccagagc ttgcggctgg agtacctgca gatcccaccg gtcagccgcg 60 cctacaccac tgcctgcgtc ctcaccaccg ccgccgtgca gttggaattg atcacacctt 120 ttcagttgta cttcaatcct gaattaatct ttaaacactt tcaaatatgg agattaatca 180 ccaacttctt attttttggg ccagttggat tcaatttttt atttaacatg atttttctat 240 atcgttactg tcgaatgcta gaagaaggct ctttccgagg tcggacagca gactttgtat 300 ttatgttcct ttttggtgga ttcttaatga ccctttttgg tctgtttgtg agcttagttt 360 tcttgggcca ggcctttaca ataatgctcg tctatgtgtg gagccgaagg aacccctatg 420 tccgcatgaa cttcttcggc cttctcaact tccaggcccc ctttctgccc tgggtgctca 480 tgggattttc cttgttgttg gggaactcaa tcattgtgga ccttttgggt attgcagttg 540 gacacatata ttttttcttg gaagatgtat ttcccaatca acctggtgga ataagaattc 600 tgaaaacacc atctattttg aaagctattt ttgatacacc agatgaggat ccaaattaca 660 atccactacc tgaggaacgg ccaggaggct tcgcctgggg tgagggccag cggcttggag 720 gttaaagcag cagtgccaat aatgagaccc agctgggaag gactcggtga tacccactgg 780 gatcttttat cctttgttgc aaaagtgtgg acacttttga cagcttggca gattttaact 840 ccagaagcac tttatgaaat ggtacactga ctaatccaga agacatttcc aacagtttgc 900 cagtggttcc tcactacact ggtactgaaa gtgtaatttc ttagagccaa aaaactggag 960 aaacaaatat cctgccacct ctaacaagta catgagtact tgatttttat gggtataagg 1020 cagagccttt tcttcctctt cttgatagat gaggccatgg gtgtaaatgg aagtttcaga 1080 gaggacaaaa taaaacggaa ttccattttt ctctcactgt aaaaaaaaaa aaaaaa 1136 <210> SEQ ID NO 114 <211> LENGTH: 239 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 114 Met Ala Tyr Gln Ser Leu Arg Leu Glu Tyr Leu Gln Ile Pro Pro Val 1 5 10 15 Ser Arg Ala Tyr Thr Thr Ala Cys Val Leu Thr Thr Ala Ala Val Gln 20 25 30 Leu Glu Leu Ile Thr Pro Phe Gln Leu Tyr Phe Asn Pro Glu Leu Ile 35 40 45 Phe Lys His Phe Gln Ile Trp Arg Leu Ile Thr Asn Phe Leu Phe Phe 50 55 60 Gly Pro Val Gly Phe Asn Phe Leu Phe Asn Met Ile Phe Leu Tyr Arg 65 70 75 80 Tyr Cys Arg Met Leu Glu Glu Gly Ser Phe Arg Gly Arg Thr Ala Asp 85 90 95 Phe Val Phe Met Phe Leu Phe Gly Gly Phe Leu Met Thr Leu Phe Gly 100 105 110 Leu Phe Val Ser Leu Val Phe Leu Gly Gln Ala Phe Thr Ile Met Leu 115 120 125 Val Tyr Val Trp Ser Arg Arg Asn Pro Tyr Val Arg Met Asn Phe Phe 130 135 140 Gly Leu Leu Asn Phe Gln Ala Pro Phe Leu Pro Trp Val Leu Met Gly 145 150 155 160 Phe Ser Leu Leu Leu Gly Asn Ser Ile Ile Val Asp Leu Leu Gly Ile 165 170 175 Ala Val Gly His Ile Tyr Phe Phe Leu Glu Asp Val Phe Pro Asn Gln 180 185 190 Pro Gly Gly Ile Arg Ile Leu Lys Thr Pro Ser Ile Leu Lys Ala Ile 195 200 205 Phe Asp Thr Pro Asp Glu Asp Pro Asn Tyr Asn Pro Leu Pro Glu Glu 210 215 220 Arg Pro Gly Gly Phe Ala Trp Gly Glu Gly Gln Arg Leu Gly Gly 225 230 235 <210> SEQ ID NO 115 <211> LENGTH: 1617 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1164) <400> SEQUENCE: 115 tgttgtgtgg gtggcatttt tcttaacgag atttgcttct gtcttagcct cacacaggga 60 aaatatccat ttatcttctc tctcgtgctt aattaatagc tttatctttt tttataccat 120 tttatccttt tctctttaac agaaagtaaa tatgtataaa atttgaagga atcgaactaa 180 caatacattc tgtgtatatt attttaatga agaaaataaa ttgattactg gcattggaac 240 agtataaaat accagtttgt acagtatgac ctatatgtga ccatgttact cccttccatt 300 tcacacaaag aaatagacac aactgcagtt cacaagtagt actggctcca ccccttggtg 360 ctggcagtgt ttggggacat tatgctggaa agagctccta gcatcagagg attaacacta 420 gcagattctg ttccatcttt gcactgttgc ttacctgctg attttcttaa ctgttcttgt 480 gcaatcgaca atgtgctaac ctgcttttct ctttttgtaa acgtttttgc attacaggct 540 gcattcttgc cttactgtat agaaaaagaa aaaaggctgg gtttactatt gcacatttta 600 agcttttata cctttatctt cttggaatgg tcagattctg aactggacag tcagaaccac 660 aggtctgctg ttaagggatt ttaaattgtg catttttaac cctacagtga aataacttaa 720 gatatccctg tgttcacagt gtgaggggct gttttatgtc atgttggcat aaattgtttt 780 gtaaaaggga aagtgtttct aaaggtgttt cagcgcttgt gctgatacaa agtaagttat 840 tactttgcac caggtggttt ggccactgaa ttaatactgt atagcaagag aaacaatctt 900 atttttttgg acaacatgtt ttattaagtt cttcatttct gttgattttt ttattgcatt 960 tatgattcag tggctgggaa ttgagaattt atttgaaata gaataggtaa cacctcagcg 1020 tactatagaa aatgcactca gctcaactgc tgtgtttaaa atacacattt taaatccctc 1080 tttacagaca ctaacataaa agtacatctt tctgggttgt aaacatgtgg tagtaccaga 1140 gtattgtata gtcaatgtta aatnaaagcc aaaactggaa tgtgcagaaa gtaggctttg 1200 gttaatttgt ggattcattt ttatttttgt ctttgtttaa ctttttaaaa aataagattt 1260 ctggagtaga ttggtatatt ctgttaaaga cttacagtga tccattttgc ttacactgtt 1320 gcatcacaag ggactcaccc agggaccatg acctgctggt gtgtgtgtat atttacaaaa 1380 acaaaacaaa caaaccaccc attgggatat aaggtagcaa tcacaaacta aagactgcgg 1440 cttgttgagg tgcaataccc tgactcccaa agttagttac agtgggtttt attgtttttg 1500 tgactgaagg atttattcag actgctgtac tcttcatttg atgtaacaaa atgctattaa 1560 tctaaatatt tgtaaataaa gtacctgtat ctagattaaa ttaaaaaaaa aaaaaaa 1617 <210> SEQ ID NO 116 <211> LENGTH: 100 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 116 Met Leu Glu Arg Ala Pro Ser Ile Arg Gly Leu Thr Leu Ala Asp Ser 1 5 10 15 Val Pro Ser Leu His Cys Cys Leu Pro Ala Asp Phe Leu Asn Cys Ser 20 25 30 Cys Ala Ile Asp Asn Val Leu Thr Cys Phe Ser Leu Phe Val Asn Val 35 40 45 Phe Ala Leu Gln Ala Ala Phe Leu Pro Tyr Cys Ile Glu Lys Glu Lys 50 55 60 Arg Leu Gly Leu Leu Leu His Ile Leu Ser Phe Tyr Thr Phe Ile Phe 65 70 75 80 Leu Glu Trp Ser Asp Ser Glu Leu Asp Ser Gln Asn His Arg Ser Ala 85 90 95 Val Lys Gly Phe 100 <210> SEQ ID NO 117 <211> LENGTH: 849 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 117 gaataattgt tatctttaac acttggatgt tttgttttaa tcagacatcc agacctgcca 60 agatacttag atgactctgt ccctgggctc taaagatggg atgagtgggc ttcccacctc 120 actaacctgc accccacatt ttctgactag accaggcatt ctggggcagc tgcctgaggc 180 tgtgtgcttg ttaaggctcc aaacccacct ctctttccca ggctgggtcc ctcacacccc 240 tcctcttctt atgtatcacc acctgctccc ttcaaccagc ccagtttgtt cacctcttcc 300 tagatccacc ctccttgctc tgtttcctac atgtctgccc atccccacct ccttcaagtc 360 cctataaagc tcatggccat gtccattctc ctccagactt ctcccctagt aatcttaaac 420 acaacaataa ctaacactta ttaagcacat attacatccc aagtcctgtt actcgtttca 480 tttaatcctt ataactaccc gtgagggtag acttattatt aaccccattt gagagaggaa 540 aaaaattaag gatcgaaaag gtgaagaaac ctactcaagg tcaaacaatt tctaagtggc 600 aaagccaggc ttcgcattca agtctgtcat atgtatttca tgccccttat ccctatctga 660 tattatacta catatttatt catgtattca tttggttgtt attatctaga atgtaggctt 720 cctaagggca gaggttatct tatttagcat ttcctatatc agtacctgct acataattga 780 tgctcaataa atatttaagt gaataaatga attgatggca aaaaaaaaaa aaaaaaaaaa 840 aaaaaaaaa 849 <210> SEQ ID NO 118 <211> LENGTH: 98 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 118 Met Thr Leu Ser Leu Gly Ser Lys Asp Gly Met Ser Gly Leu Pro Thr 1 5 10 15 Ser Leu Thr Cys Thr Pro His Phe Leu Thr Arg Pro Gly Ile Leu Gly 20 25 30 Gln Leu Pro Glu Ala Val Cys Leu Leu Arg Leu Gln Thr His Leu Ser 35 40 45 Phe Pro Gly Trp Val Pro His Thr Pro Pro Leu Leu Met Tyr His His 50 55 60 Leu Leu Pro Ser Thr Ser Pro Val Cys Ser Pro Leu Pro Arg Ser Thr 65 70 75 80 Leu Leu Ala Leu Phe Pro Thr Cys Leu Pro Ile Pro Thr Ser Phe Lys 85 90 95 Ser Leu <210> SEQ ID NO 119 <211> LENGTH: 925 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (883) <400> SEQUENCE: 119 cgcatcgtcg tcctccccga ccgcgtcctg cagcagctgc cagtggagcc gcctgacaag 60 gactgccatc caccatggtg aagctgggct gcagcttctc tgggaagcca ggtaaagacc 120 ctggggacca ggatggggct gccatggaca gtgtgcctct gatcagcccc ttggacatca 180 gccagctcca gccgccactc cctgaccagg tggtcatcaa gacacagaca gaataccagc 240 tgtcctcccc agaccagcag aatttccctg acctggaggg ccagaggctg aactgcagcc 300 acccagagga agggcgcagg ctgcccaccg cacggatgat cgccttcgcc atggcgctac 360 tgggctgcgt gctgatcatg tacaaggcca tctggtacga ccagttcacc tgccccgacg 420 gcttcctgct gcggcacaag atctgcacgc cgctgaccct ggagatgtac tacacggaga 480 tggaccccga gcgccaccgc agcatcctgg cggccatcgg ggcctacccg ctgagccgca 540 agcacggcac ggagacgccg gcggcctggg gggacggcta ccgcgcagcc aaggaggagc 600 gcaaggggcc cacccaggct ggggcggcgg cggcggccac cgaacccccc gggaagccgt 660 cggccaaggc ggagaaggag gcggcgcgga aggcggccgg gagcgcggcg cccccgcccg 720 cgcagtgacg tctccagccc cgcagcccgg cccgggcgtc ctccgccagc tcctgtgacc 780 agcgcgtctc ccgatgctct ccgccgtgtt cgtgtcccca ggcgccctcg ctgcagcccc 840 gcgccccgtg ggtctctgac tctgtcgctt ttctctaagt aangatttca cgtccaaaaa 900 aaaaaaaaaa aaaaaaaaaa aaaaa 925 <210> SEQ ID NO 120 <211> LENGTH: 217 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 120 Met Val Lys Leu Gly Cys Ser Phe Ser Gly Lys Pro Gly Lys Asp Pro 1 5 10 15 Gly Asp Gln Asp Gly Ala Ala Met Asp Ser Val Pro Leu Ile Ser Pro 20 25 30 Leu Asp Ile Ser Gln Leu Gln Pro Pro Leu Pro Asp Gln Val Val Ile 35 40 45 Lys Thr Gln Thr Glu Tyr Gln Leu Ser Ser Pro Asp Gln Gln Asn Phe 50 55 60 Pro Asp Leu Glu Gly Gln Arg Leu Asn Cys Ser His Pro Glu Glu Gly 65 70 75 80 Arg Arg Leu Pro Thr Ala Arg Met Ile Ala Phe Ala Met Ala Leu Leu 85 90 95 Gly Cys Val Leu Ile Met Tyr Lys Ala Ile Trp Tyr Asp Gln Phe Thr 100 105 110 Cys Pro Asp Gly Phe Leu Leu Arg His Lys Ile Cys Thr Pro Leu Thr 115 120 125 Leu Glu Met Tyr Tyr Thr Glu Met Asp Pro Glu Arg His Arg Ser Ile 130 135 140 Leu Ala Ala Ile Gly Ala Tyr Pro Leu Ser Arg Lys His Gly Thr Glu 145 150 155 160 Thr Pro Ala Ala Trp Gly Asp Gly Tyr Arg Ala Ala Lys Glu Glu Arg 165 170 175 Lys Gly Pro Thr Gln Ala Gly Ala Ala Ala Ala Ala Thr Glu Pro Pro 180 185 190 Gly Lys Pro Ser Ala Lys Ala Glu Lys Glu Ala Ala Arg Lys Ala Ala 195 200 205 Gly Ser Ala Ala Pro Pro Pro Ala Gln 210 215 <210> SEQ ID NO 121 <211> LENGTH: 1645 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 121 caaaaacctg tgactatact ttctattggg caaggctctc tactcctgtg acttctgtct 60 gccctgatag ctggtagcat tttcctgggt acctgccata tgccaggcac aatagaacct 120 tatcttcttc ccatttcaca gagaagaaag gtgaggctcg gagagggaaa gtgacttgcc 180 caagcttgag ctgctgggaa aaatgccagg gaccaggata cagaccttgg tcatctgact 240 ccaaagtccc ccgtgatgtt ttctgtgttt ggtggcctgt tggtgagggg ccctgccctc 300 agaacacccc tctgccagag caagatgtgt gagcacatcc ctgaagccag caagcctgca 360 gctagcggta tcattaccat catggtagcc ggagccaggg gtgccatctg ccagcaggga 420 gagaagtatg cacatctcag agtaggggtg ttagagaaac atcgccatgg ggctgacagc 480 caggtaggat ggcaggagtc acctggggtg aggaggggca ggtgctctag gcagaaaaaa 540 ccgcagcagc aaaggtgtgg aggtggaagg atcagggctc tgctgagaga atgtatagtt 600 ggggcttcag tgcaggagag agcactgaga gatgaggtca gaggcccgag agggagtcag 660 cctggggcat gcaaagctgc gaggcactgg ggagccatgg aaggttcaag caggagagag 720 gcctgctctg gttggtgctt caggaaactc ccccagctga caggtttgga gggcagtgtg 780 taagcagaga gtgaggcaag gtggcagctg caggcaggag atggttggta tgtgggccag 840 ggtggggtag tggggcagga gaaaagtggg cagactttgg aggcagcctc ttccctcctt 900 ggtgcctggg ctgactgtgg gggatgggga ggagggaaga gtgacctgga atgcccgggg 960 ctggcttgga tgcaatggcc ctgcccttct aaggaggtga ggaacagaaa agctaccaag 1020 gtctgggggt cacagataag tgtgtggggg gcctaagaga ctcccaggct gtagcacgaa 1080 ggctccaaga agtggtggct cagccctgtg gcccaccaga cctgattcag cttccaggcc 1140 cagtcgccca gccccccagt tgagtggcag ctgtcacaga acccaatgtc tccccgcacc 1200 atgtccaaat aaaggaaaaa ccaaaatacg tttccctttg tccgaatcca gcgagggtga 1260 gttgggcgag agtcatccgc tattgtgtgc tgaggcccac actgcttctt acataagccc 1320 cgagttaaaa atatgcccgg aattctcatt ctcaagctct gcctgggatt gcaccctgac 1380 ccccagcctc ggcagcttct agcacccaca gggatgaaga aactgcccca tggcacaacg 1440 ctggcacgtg gcacttctag ctctgtctgc ctccagtgcc acgaacagta agagtgcgcc 1500 gggtgcggtg ctcacgcctg taatcccagc actttgggag gccaaggtgg gcagatcact 1560 tgagcccagg agtttgagac cagcctgggc gaacatagca agaccccatc tctacaaaaa 1620 aaaaaaaaaa aaaaaaaaaa aaaaa 1645 <210> SEQ ID NO 122 <211> LENGTH: 175 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 122 Met Phe Ser Val Phe Gly Gly Leu Leu Val Arg Gly Pro Ala Leu Arg 1 5 10 15 Thr Pro Leu Cys Gln Ser Lys Met Cys Glu His Ile Pro Glu Ala Ser 20 25 30 Lys Pro Ala Ala Ser Gly Ile Ile Thr Ile Met Val Ala Gly Ala Arg 35 40 45 Gly Ala Ile Cys Gln Gln Gly Glu Lys Tyr Ala His Leu Arg Val Gly 50 55 60 Val Leu Glu Lys His Arg His Gly Ala Asp Ser Gln Val Gly Trp Gln 65 70 75 80 Glu Ser Pro Gly Val Arg Arg Gly Arg Cys Ser Arg Gln Lys Lys Pro 85 90 95 Gln Gln Gln Arg Cys Gly Gly Gly Arg Ile Arg Ala Leu Leu Arg Glu 100 105 110 Cys Ile Val Gly Ala Ser Val Gln Glu Arg Ala Leu Arg Asp Glu Val 115 120 125 Arg Gly Pro Arg Gly Ser Gln Pro Gly Ala Cys Lys Ala Ala Arg His 130 135 140 Trp Gly Ala Met Glu Gly Ser Ser Arg Arg Glu Ala Cys Ser Gly Trp 145 150 155 160 Cys Phe Arg Lys Leu Pro Gln Leu Thr Gly Leu Glu Gly Ser Val 165 170 175 <210> SEQ ID NO 123 <211> LENGTH: 2515 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 123 ctttgggtaa tggaggaggt tgcagttccc gtgctgtaat tagacatctt ttaattagac 60 atcttttcca gcagagccat ttaaaatatt ttcctagagg acctgccccc taacctcagc 120 cagtcaatgg ggaggagttt tgaatgccac actccccagt ttgccaccaa accacaggca 180 gagagttgtg ttcatcacac tagacagaaa tctgtgtcag tcagggtcct tgcccatatg 240 tctccccttt gtccccctct gtacgggatt caatcaatgt ttgtcaaagc atatcattac 300 gtaaactgtc agaatatggt gctgagtagg aatggcaccg cgttattcat tcagtccctt 360 tatcgaggat ctaccatgca cctacattta tctaaatcta attattagta cacattttca 420 aatttgaact tctatgtgga gaggtacata aaaatataaa ttattggctg ggtgtggtgg 480 ctcacattta taatccttat aagcccagca ctttgggagg ccaaggtgcc tggattgctt 540 gagcctagga attcgaggcc agcctgggca acatggtgaa accctgtctc tacaaaaaat 600 ttaaaaatta gctgggcatg gtggcatgca cctgtagtcc cagctactag ggaggctgag 660 gtgggaagat cgcttgagcc ctggaggcag aggttgcagt gagctatgat tgtaccactg 720 cactctagtc tgggcaagag aagagaacct gtctcaaaaa atgtgtatat taaaaacata 780 taaatccttg ctcataacag aaaacagtag catatatgga aattaatcaa acctcttcca 840 actcttccct ctttgacaca tggaatttcc aagcaagttg tatcactggt ctactttaag 900 ggccatctca agtgggagac ataaaggtgt tttcccatct atgggaatat tgacaagagc 960 taacagaagg aatttcaaaa ggttccacag tcacagagca accaacagga agtgaaggca 1020 ggaagattcc tcatcaactc tattagtaca gcagaacagc aagatgaatg ttatgaagaa 1080 gttgagtcat tttctactgg tacttaggtc cacccggacc ttatcccttc actccccatt 1140 catcagccac atcctttgtg tcttgcctgc cctgctgtgg aatatgccat gagaatcatg 1200 tatatccagc ttcatcagct actgtcagct tgggaagacc cagtttcctt gaggttgacg 1260 tcctgtttca gaacaaatca ctggacttct tcagcataac atggcttttg ataagaagaa 1320 attctccatt tctttaagta tcctctgtag aaacagttta tataaagtcc ttggggtgac 1380 ctcaatccca tccacagctt caatttatga gatgatgact cagaccacat ttctggctca 1440 gaactttata tcaggctcca gatccatgtt ttcaaatgcc ttgaacatcc caagggtggc 1500 ttgaacttga actcacctca ctgcccccgc tttctgtcct aaatctaaat tttagtaaat 1560 tatagcatta catatctaat gataggttca caaaccagca attggaagca tccacagtag 1620 gtgaggcacg agcaggctgg ctttggtctg ctggaatctg gtttatttga aactaatgcc 1680 aagacacagc ttcctcttac tctcccaccc caggcaattg ctcttgcctt ggctgtgtcc 1740 tacaggctgc ctcattctcc tctcctgccc ctgcttccac ccacctggaa tcacttctcc 1800 aggtcataca aagcaccttt gccccacaca aggattcaag caggctgacc aacagaagtc 1860 atcttgagga tcttgtgaaa actatagatt cccatgctct tccccacgac cctctgattc 1920 tgggagtcta ggttgagacc taatccaccg tggggaccat cagagaattc agtctgtgcc 1980 ctagtgcaca acatgaaaaa aactatgatg ttctgtgtct ccccacaagt ttggagtact 2040 gttctcacaa gcattgatgg cactacacac acacatcaca cacatgcaca aatgcatcca 2100 cacacatgca caaatacaaa tgcatacatg tgtgacacaa atgcatttta gtcatactgt 2160 cactgtgccc aggtctcctt ccgttgtttc tacaaataat cattgagtaa acaatcatct 2220 actaagccat tcggagctcc cagctctgct cgcgcattgc cagacttgcc ccttccccct 2280 gatgaccacg gcaccctcct gactggtctc cctccctctg ggctgccctc tacacttctg 2340 acttagtggt ctttggaaat gcagattgag gtcaccgaag tgccttgacc ctacatgaag 2400 gtcaaacttc tcagctctga aaacagtgct tgcccagtgt ctggggcttc atttggtctg 2460 ccctccgaca gccgctcctc aatgcgccac caccacgaaa caaaaaaaaa aaaaa 2515 <210> SEQ ID NO 124 <211> LENGTH: 93 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 124 Met Gly Arg Ser Phe Glu Cys His Thr Pro Gln Phe Ala Thr Lys Pro 1 5 10 15 Gln Ala Glu Ser Cys Val His His Thr Arg Gln Lys Ser Val Ser Val 20 25 30 Arg Val Leu Ala His Met Ser Pro Leu Cys Pro Pro Leu Tyr Gly Ile 35 40 45 Gln Ser Met Phe Val Lys Ala Tyr His Tyr Val Asn Cys Gln Asn Met 50 55 60 Val Leu Ser Arg Asn Gly Thr Ala Leu Phe Ile Gln Ser Leu Tyr Arg 65 70 75 80 Gly Ser Thr Met His Leu His Leu Ser Lys Ser Asn Tyr 85 90 <210> SEQ ID NO 125 <211> LENGTH: 1763 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 125 gcctcagcaa caaagaaaaa gtgaattttt aatgctgaag ataaagtaag ctaaagtacc 60 agcagaagcc ttggctattt atagcagttc tgacaatagt tttataagaa catgaagaga 120 acagaatcac ttgaaaatgg atgccagtca tctcttgttc ccactactga attcttataa 180 agtggtggca agatagggaa gggataatct gagaattttt aaaagatgat ttaatgagaa 240 gaagcacaat tttgattgtg atgagtcact ttctgtaaac aatcttggtc tatctttacc 300 cttatacctt atctgtaatt taccatttat tgtatttgca aagcgagtag gggttgaatc 360 acaggaaatc ctttgtattc cagactttag ggcagagcct gagggagtat tattttacat 420 aacccgtcct agagtaacat tttaggcaac attcttcatt gcaagtaaaa gatccataag 480 tggcatttta cacggctgcg agtattgtta tatctaatcc tattttaaaa gatttttggt 540 aatatgaagc ttgaatactg gtaacagtga tgcaatatac gcaagctgca caacctgtat 600 attgtatgca ttgctgcgtg gaggctgttt atttcaacct ttttaaaaat tgtgtttttt 660 agtaaaatgg cttatttttt cccaaaggtg gaatttagca ttttgtaatg atgaatataa 720 aaatacctgt catccccaga tcatttaaaa gttaactaaa gtgagaatga aaaaacaaaa 780 ttccaagaca ctttttaaaa gaatgtctgc cctcacacac ttttatggat ttgtttttct 840 tacataccca tcttttaact tagagatagc attttttgcc ctctttattt tgttgtttgt 900 ttctccagag agtaaacgct ttgtagttct ttctttaaaa aacatttttt ttaaagaaga 960 agaagccact tgaaccctca ataaaggctg ttgcctaagc atggcatact tcatctgttc 1020 tcatttgtgc catctgccgt gatgtcgtca cttttatggc gttaatttcc tgccactaca 1080 gatcttttga agattgctgg aatactggtg tctgttagaa tgcttcagac tacagatgta 1140 attaaaggct tttcttaata tgttttaacc aaagatgtgg agcaatccaa gccacatatc 1200 ttctacatca aatttttcca ttttggttat tttcataatc tggtattgca ttttgccttc 1260 cctgttcata cctcaaattg attcatacct cagtttaatt cagagaggtc agttaagtga 1320 cggattctgt tgtggtttga atgcagtacc agtgttctct tcgagcaaag tagacctggg 1380 tcactgtagg cataggactt ggattgcttc agatggtttg ctgtatcatt tttcttcttt 1440 ttcttttcct ggggacttgt ttccattaaa tgagagtaat taaaatcgct tgtaaatgag 1500 ggcatacatg catttgcaac aaatattcaa atagaggctc acagcggcat aagctggact 1560 ttgtcgccac tagatgacag gatgttataa ctaagttaaa ccacatctgt gtatctcagg 1620 ggacttaatt cagctgtctg tagtgaataa aagtgggaaa ttttcaaaag tttctcctgc 1680 tggaaataag gtataatttg ttttttgcag acaattcggt aaagttactg gctttcttgg 1740 tgaaaaagaa aaaaaaaaaa aaa 1763 <210> SEQ ID NO 126 <211> LENGTH: 102 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 126 Met Trp Ser Asn Pro Ser His Ile Ser Ser Thr Ser Asn Phe Ser Ile 1 5 10 15 Leu Val Ile Phe Ile Ile Trp Tyr Cys Ile Leu Pro Ser Leu Phe Ile 20 25 30 Pro Gln Ile Asp Ser Tyr Leu Ser Leu Ile Gln Arg Gly Gln Leu Ser 35 40 45 Asp Gly Phe Cys Cys Gly Leu Asn Ala Val Pro Val Phe Ser Ser Ser 50 55 60 Lys Val Asp Leu Gly His Cys Arg His Arg Thr Trp Ile Ala Ser Asp 65 70 75 80 Gly Leu Leu Tyr His Phe Ser Ser Phe Ser Phe Pro Gly Asp Leu Phe 85 90 95 Pro Leu Asn Glu Ser Asn 100 <210> SEQ ID NO 127 <211> LENGTH: 1698 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 127 caaagaaaag gttggttaga ataagtaaaa tttcagttag aaagatatag cttaccagtt 60 ttccatgtgc ttaaggaagt caagaatatt tcaggttgtt gagaactgtt gtaaaatgga 120 attgaagcta gtgtctctca ccttcttagg tgtatcagag agaggaagtg gaaggccagt 180 agtagcatct tcatacttac ttttgccagc ccagcctcca tttcaaagac tttgtcttcc 240 atcctatcca atgacatggt cagggatggg ctctgaggag gcagtgaggc cccaccttgg 300 tttgctccac tgtggtgtgt agtctccaaa cagcttaagg gtttttaagt tttctcacga 360 ttacctccac tccactcatc tactatcagc atcagaaagg ttaacatccc tgggaccatt 420 ctacttataa aagagatgaa ctagtgtgct ttctcccctt ttccaggtgt gccatccata 480 tacaatctcc tcttggccaa gttcaacaaa tgtttccagg gaaccccgtg ggttgaggca 540 aagtagccaa gatgtattga gttaagtttt tctagaggac aaaagtattt cttgtccctt 600 ttccctcatg ctcatatgtt ttagctgagg cgtaaatggc caagttgagt aatatctgtg 660 gaactgagac agagagccag ggacccatgt acccagggac cagtcccctg gggaatcaca 720 cagtggctca gactagactg ctctatccca ccagaactct gctgctgttc atttccatca 780 ggaccaccca ggaaagcaaa taagttagcc ttctcatcat taggtcacct aatctcttgg 840 ggtgcaggat gagagcatat atagatctcc tgtttagaga gtgtgttcat aattgtagaa 900 agggatagaa aatggaataa ccaagaggct gtgtcatttt ttaagaggat ggcaaggatg 960 acctcaaatg agctcaacaa aactgggaat ccaaggaatg gtgcttgtag ggaaagagag 1020 gtcagttgtg gtccttaaac ctcttggcac cttgtgcggg ttataaaaca aggagctgga 1080 gtaaaattgc ccttaccccc aatccaaatg ctgtccagga tttaggagct acccaacctg 1140 tggttatatg gtgttggttt ccattttttg tttgtttgct tgtttccaaa atagccttgc 1200 ttggtactgc atggaaagtt caagcttttc ttcttgcccg ctcagggctg gcctcttccc 1260 cgtgtcttca cagcgtccct aaggaagatt tttgcagcac tctctggagc tgaggggagt 1320 gaaatttggt ccagagaagg cggaaggaaa tagttttcct gtttcctttt ctcgaggtgg 1380 atgtcctcag gcttccttca cacctccttc tcatgggtgc ggctggcagt acagtcaggc 1440 tgtggaggag ggctgagaag aaaggggcac tggtccagcc ccaggtttgg tctgagacag 1500 gtacacagca gataccatcc caccttcctc tctaaagaac aggccagcca cacatataac 1560 cctttcccta ctttactaat gtatccctta tgtggtacca gcaatggagg acaggcagac 1620 ttaccccctg ccatctagag agaatgttgt tattacccgt aaaacttgac caccccacga 1680 aacaaaaaaa aaaaaaaa 1698 <210> SEQ ID NO 128 <211> LENGTH: 85 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 128 Met Cys Leu Arg Lys Ser Arg Ile Phe Gln Val Val Glu Asn Cys Cys 1 5 10 15 Lys Met Glu Leu Lys Leu Val Ser Leu Thr Phe Leu Gly Val Ser Glu 20 25 30 Arg Gly Ser Gly Arg Pro Val Val Ala Ser Ser Tyr Leu Leu Leu Pro 35 40 45 Ala Gln Pro Pro Phe Gln Arg Leu Cys Leu Pro Ser Tyr Pro Met Thr 50 55 60 Trp Ser Gly Met Gly Ser Glu Glu Ala Val Arg Pro His Leu Gly Leu 65 70 75 80 Leu His Cys Gly Val 85 <210> SEQ ID NO 129 <211> LENGTH: 2110 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 129 agcagagaag attgaagatg tggaaatcac actggtgtga tgatgggctt gcccatccat 60 tactgctaca atcaaggcca ggcttggagt ttggccagtc ttgtttttta ggcacctttg 120 catgatgatg actcttgaac agagcaaaaa acaaggagga ttatgtgtga ctgggtggcc 180 tggtagactc ctcccacgtt ttgaatattt cgtgcctttt ttttttgttg tcattttcta 240 tgtcatttct cctaccatag cacaaatcct agcggaccct atgatcaaag aggggggcag 300 cctcatgcct aacagtggtc tgttttatat gaagactcaa gaacaagcct cattccaggg 360 cacagtccct aaattactga tcatgtgcac tcgtacagta tattactgtg accacaaggg 420 atgtggcaaa gattctcatc tttcttcaag tggcttttgc tcatctgatt gagaattaat 480 cagatcatgt tggctacata aggaaacaga aggagggatt tcaggagagg ctggctcctc 540 cccaaggtta gtccccagac tgagaaagtg aaaccttatt gggaaaaatt ggactgccct 600 gaatttagca ccaattgcat taacgcacat ctcttccaca actaacagac ttaaaataac 660 agtgtccttc gtattaatat ctgtgccatt catttagaat tagcagagct aatatggagg 720 ggctgaacta gtagccacat cttgttcatc acatagacta atagaaagga gctgtggcta 780 aagcagaaat ggaacttccg gatctgaaat tagcccatat aatgttcttt tgtatttggg 840 tatttttcat cttaattttt acagcatata ctcttcttac cagtatcctt agaatccaaa 900 tgtctagata agttgaggac acatacctgc attgttgagc ttctctactg gggacgcccc 960 ggcattattt tattcccaag ccagcagacc ggcccagaca gccaggctgt ggctggtcca 1020 gaccaactgc tatggtggaa aatgcagctt ccaggtccca ctaccctgac atttccgtgg 1080 aaggaagaac ctggtggctc gtggaggaaa ccagctttct atgagaaagg actgaaggat 1140 tgcgcaccct gcacaagtac agattgacca ggaaaagaca agtgtcttct gtgtgtcaca 1200 gggaaagcca ggagtggcct tctctgcaac cagcaagcct gcagcaacag gtgcccccac 1260 gtcaggtgct gactgttcgc tgtccgctcc tgtagaaagt tgggagcaca atacctatgg 1320 acttaaggat gttcgccggt tgtgggttgg gttttttttt tttcctgggg taagaaatcg 1380 aatttgcgga atttaaatct tccaggttgt ataatgcttt gaaaactcca tccctcctaa 1440 agaatcataa aaaaacttga aatgctcgcc aaatgtcccc catggggatt tttgaccaaa 1500 aggtaaggtg ataacaggag aaatttttgg ttctttgatc acttcagtga caataccctt 1560 taatgcatct tctccatgat ttggggtttt ttttcgttgt tgttttttac acttcttaac 1620 ctgttgatct atttgaggtc tttggtgttt atcaaactaa ttcttaagtt taaaaaagaa 1680 attaaaaggg tggttttttt aagattttaa agtttgctaa catattaaaa atcttcaaat 1740 gcttattaaa tagagcagtt cttgccaccc agtctggtat tctgtcttta gctagccaaa 1800 ttgtccttga atttgggttt tccacaacct caaagggtta tttgaaatct tttgtagtat 1860 tttaaaatat tttttggaag agctgctaat tttattttaa aaaacagagt tgtgaaaaca 1920 tgcctccttt ttaaaaaata acccctccat ccaggatatg gaatccagca ccacagtgca 1980 caggtcaggg ctcggaggga gcctctgtgc agatgtgctt tctttacagt ggctgtaaaa 2040 agtttgtatt tactatgtat aaaatgttga ataataaaaa aaatggaatt aaaaaaaaaa 2100 aaaaaaaaaa 2110 <210> SEQ ID NO 130 <211> LENGTH: 116 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 130 Met Met Met Thr Leu Glu Gln Ser Lys Lys Gln Gly Gly Leu Cys Val 1 5 10 15 Thr Gly Trp Pro Gly Arg Leu Leu Pro Arg Phe Glu Tyr Phe Val Pro 20 25 30 Phe Phe Phe Val Val Ile Phe Tyr Val Ile Ser Pro Thr Ile Ala Gln 35 40 45 Ile Leu Ala Asp Pro Met Ile Lys Glu Gly Gly Ser Leu Met Pro Asn 50 55 60 Ser Gly Leu Phe Tyr Met Lys Thr Gln Glu Gln Ala Ser Phe Gln Gly 65 70 75 80 Thr Val Pro Lys Leu Leu Ile Met Cys Thr Arg Thr Val Tyr Tyr Cys 85 90 95 Asp His Lys Gly Cys Gly Lys Asp Ser His Leu Ser Ser Ser Gly Phe 100 105 110 Cys Ser Ser Asp 115 <210> SEQ ID NO 131 <211> LENGTH: 752 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 131 cccgtgtttc ccgggctggg tatttgcctc gcaccatggc gcccaagggc aaagtgggca 60 cgagagggaa gaagcagata tttgaagaga acagagagac tctgaagttc tacctgcgga 120 tcatactggg ggccaatgcc atttactgcc ttgtgacgtt ggtcttcttt tactcatctg 180 cctcattttg ggcctggttg gccctgggct ttagtctggc agtgtatggg gccagctacc 240 actctatgag ctcgatggca cgagcagcgt tctctgagga tggggccctg atggatggtg 300 gcatggacct caacatggag cagggcatgg cagagcacct taaggatgtg atcctactga 360 cagccatcgt gcaggtgctc agctgcttct ctctctatgt ctggtccttc tggcttctgg 420 ctccaggccg ggccctttac ctcctgtggg tgaatgtgct gggcccctgg ttcactgcag 480 acagtggcac cccagcacca gagcacaatg agaaacggca gcgccgacag gagcggcggc 540 agatgaagcg gttatagcca ttgacattat tgccacaggc cactggccct gggtggctct 600 gtcagggtgc acagcccctc atgcctggag caatgagggt ttagtccagg ggccaaaagc 660 agtctgaggt attgggtata cttatactct atagggtcgt tgaataaatg gcttagaatg 720 tgaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 752 <210> SEQ ID NO 132 <211> LENGTH: 173 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 132 Met Ala Pro Lys Gly Lys Val Gly Thr Arg Gly Lys Lys Gln Ile Phe 1 5 10 15 Glu Glu Asn Arg Glu Thr Leu Lys Phe Tyr Leu Arg Ile Ile Leu Gly 20 25 30 Ala Asn Ala Ile Tyr Cys Leu Val Thr Leu Val Phe Phe Tyr Ser Ser 35 40 45 Ala Ser Phe Trp Ala Trp Leu Ala Leu Gly Phe Ser Leu Ala Val Tyr 50 55 60 Gly Ala Ser Tyr His Ser Met Ser Ser Met Ala Arg Ala Ala Phe Ser 65 70 75 80 Glu Asp Gly Ala Leu Met Asp Gly Gly Met Asp Leu Asn Met Glu Gln 85 90 95 Gly Met Ala Glu His Leu Lys Asp Val Ile Leu Leu Thr Ala Ile Val 100 105 110 Gln Val Leu Ser Cys Phe Ser Leu Tyr Val Trp Ser Phe Trp Leu Leu 115 120 125 Ala Pro Gly Arg Ala Leu Tyr Leu Leu Trp Val Asn Val Leu Gly Pro 130 135 140 Trp Phe Thr Ala Asp Ser Gly Thr Pro Ala Pro Glu His Asn Glu Lys 145 150 155 160 Arg Gln Arg Arg Gln Glu Arg Arg Gln Met Lys Arg Leu 165 170 <210> SEQ ID NO 133 <211> LENGTH: 698 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 133 ggcagccatg gtcggggcgc tgtgcggctg ctggttccgc ctgggcgggg cccgcccgct 60 catcccgttg ggcccgactg tggtacagac ctccatgagc cggtcccagg tagccctgct 120 gggcctgagt ctgctgctca tgctcctact gtatgtgggg ctgccaggcc cccctgagca 180 gacttcctgc ctctggggag accccaatgt cacagtcctg gctggtctca cccctggcaa 240 ctcgcccatc ttttaccgcg aggtgctccc acccacccag aactacaccc aggagcaatt 300 ctgggctgtg aagactccaa cccttatcct gtatggagag ctggaccaca tcctggctcg 360 agagtcactg cggcagctcc gccacctgcc caaccactct gtggtgaagc tacgcaatgc 420 aggccatgcc tgttacctcc acaagccgca agacttccac cttgtcctgc ttgccttcct 480 tgaccatcta ccttgaacta acccactccc agctcccagc ctggcatgag cttggacagt 540 ctggaccgcc accctccctg aaccagggag acagcctctg ggattggagg ccagaggcca 600 gggtcagacc cagccaggac tcctcatttc atctcacaga cacaataaaa aagcatattt 660 gtcctgccaa aaaaaaaaaa aaaaaaaaaa aaaaaaaa 698 <210> SEQ ID NO 134 <211> LENGTH: 162 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 134 Met Val Gly Ala Leu Cys Gly Cys Trp Phe Arg Leu Gly Gly Ala Arg 1 5 10 15 Pro Leu Ile Pro Leu Gly Pro Thr Val Val Gln Thr Ser Met Ser Arg 20 25 30 Ser Gln Val Ala Leu Leu Gly Leu Ser Leu Leu Leu Met Leu Leu Leu 35 40 45 Tyr Val Gly Leu Pro Gly Pro Pro Glu Gln Thr Ser Cys Leu Trp Gly 50 55 60 Asp Pro Asn Val Thr Val Leu Ala Gly Leu Thr Pro Gly Asn Ser Pro 65 70 75 80 Ile Phe Tyr Arg Glu Val Leu Pro Pro Thr Gln Asn Tyr Thr Gln Glu 85 90 95 Gln Phe Trp Ala Val Lys Thr Pro Thr Leu Ile Leu Tyr Gly Glu Leu 100 105 110 Asp His Ile Leu Ala Arg Glu Ser Leu Arg Gln Leu Arg His Leu Pro 115 120 125 Asn His Ser Val Val Lys Leu Arg Asn Ala Gly His Ala Cys Tyr Leu 130 135 140 His Lys Pro Gln Asp Phe His Leu Val Leu Leu Ala Phe Leu Asp His 145 150 155 160 Leu Pro <210> SEQ ID NO 135 <211> LENGTH: 1825 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 135 tgtgcgttat gtaggttgta atgaagctaa cagtttcagt tatgtactac tatttttgtc 60 catacttagt tcattgtaaa ctctatatta atttctttga taacatgtat ttgatttttt 120 tgcaatacgg ctttcaggtt cttgccattc ttcagattct catgcttatt cagatttctc 180 atttggctgg cattttgtta tcagtgaacc aaaattatct cattttaaat tcacataaga 240 caaaagcacc agtagtcagt attctagttc tccttactaa tttacggagg tgtgatctgg 300 gtgattttta aattaattta attatcattt catattcata gtgatgattt ttaaaatttt 360 acaaactttt cacctatata aacatcttta ttgtcaggtg tctgacaagc taatttcttt 420 gctaactatt ttagttatta atatattatg taggttgtat cagaattttg tttttcaccc 480 aatgcttttt cacaattccc aagtcaagaa ggatgcatta caatgtttac attagcatct 540 aaaggcaatg taaagtcggg aaacattttt agtatataat ttcataattc aaagacattt 600 ttaaaaaatg aatggttaaa ccagtatctc actgcattaa atgtaattca atacattaaa 660 tttagttatt agaagatgtt attacaagcc tcaacatgta acatgcttac ttacaaatca 720 aaaatctcag atcaagtggc tggaactgca ggggcctgcc aggcatctgg gtatttacat 780 gattcctttc catgtggtta tggcagagca tggccatttc aaggtagtca aacttcttac 840 acaaaagctg gcttaccaca gagtgggtat ttcaagggag ggaaacagaa gaagcaacat 900 atgtataatt ggaaacccgg aggaggaaaa agagggcagt gacaccaaac agtatttaaa 960 tatcaaaacc tataatctga aaacatactt acaggctttt gtgttctcca tttttccctt 1020 agcataatac ttttaaaatt tatagatatt gttccatata tcagtagttt gttttttttt 1080 ttggttttgc tccgttgtgt gatgtatagt catatgttta tatagttgcc cctggataga 1140 cgtttgggtt ttttacattt tgggcctatt agaataaaag ctcgtgaata ttccagtaaa 1200 aatttgtgtg tgaatatata tttttaatct tcttgggtaa atacatagaa atgcaatttc 1260 tgtgtcattt gttatgatca acttcattaa aaactgcaga ctcttttcaa aatcagccat 1320 atcattttgc attctcagga tgttacttga caacatcacc acatttggta tggtagtttt 1380 tttaaatttt agtgattctg gtggatgtat agtggtattt tttagtttga atttgaattt 1440 ctgaaataag taatgatatt gaacttgttt tgttattgtg atttgccatt tatacattat 1500 cttttttgaa gtatcttaaa atcttttgtc tgttttaaaa attaggttgt tgtcttaata 1560 ttgagttgtg agatttattt atttcatgta agggctttat catatatata ttttataaat 1620 attctctccc attttatagt ttgtcttttc atttcataat gggaaattgt ccccaaatac 1680 acttttgttg taatctattg taatcagcat tttaatgcat agttagcatt cagtaaaatt 1740 aatcaatttt gactgtacaa tctagtgagt tttgacagct gtataaagca gtttcccacc 1800 accacgaaaa aaaaaaaaaa aaaaa 1825 <210> SEQ ID NO 136 <211> LENGTH: 96 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 136 Met Lys Leu Thr Val Ser Val Met Tyr Tyr Tyr Phe Cys Pro Tyr Leu 1 5 10 15 Val His Cys Lys Leu Tyr Ile Asn Phe Phe Asp Asn Met Tyr Leu Ile 20 25 30 Phe Leu Gln Tyr Gly Phe Gln Val Leu Ala Ile Leu Gln Ile Leu Met 35 40 45 Leu Ile Gln Ile Ser His Leu Ala Gly Ile Leu Leu Ser Val Asn Gln 50 55 60 Asn Tyr Leu Ile Leu Asn Ser His Lys Thr Lys Ala Pro Val Val Ser 65 70 75 80 Ile Leu Val Leu Leu Thr Asn Leu Arg Arg Cys Asp Leu Gly Asp Phe 85 90 95 <210> SEQ ID NO 137 <211> LENGTH: 1503 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1193) <400> SEQUENCE: 137 ccagagtcca gactgacatt acagcgcaag agtttgcaag tgtgtccagc atgcaccaac 60 tgtgcagaac ttggctcggt aactttgcgt ggaaaaataa agtacatttt gaagtatctt 120 gagggttggg tcaattgaga catttctagc attacttaat gacttgcatt gtggtttttc 180 tgcaagcaac tttaatgact ttttttatac cacatggtct cccagtttct agatgaatgc 240 aacatgatga tggtgatgat gacgatgagt ttaatcattg ttcatttatt gcctttaggg 300 ctgagggaaa gggaaggttt gttttttttt ctccccattt tcccccattc tgtctttctt 360 ttggtgactt acaccacatg taatgacgct atgactaatt ctgctcccaa gcccttgtat 420 cttgggcttc attttaggct catgtgtcca gatctgcatg cattgcttgc atttttctgg 480 tatctgaatg ttggttcctt gttccaggaa ttcaacatta atttccaaaa gtatcatggg 540 acttgtgaca atacaagaca tgaatctatg tataaaattt atcggccttt ctcatttacc 600 tgctctagta ttattgtatt gtgtgtgcgt gcgtgtgtga tgtcaggctg ccacgtaaaa 660 cttcagagaa aaatcttaaa agcagaccat ccttttgcat gctctattct aagtagaatg 720 ttcaatgtaa ctgactaaaa ttgcatgtta aagatattta ggtttttttg ttttctttat 780 ttttatttgt tttcagtttc ctgtatattt gcttactgtg ccgttttagt ggttttagga 840 taaaaatgca ctggtgaagc aaatgtagtg ccaacagaag gtgattttcc agttgtaaat 900 gtcatgcagc atttgaaggg actgtgtttt cttaaaaaaa aaatcacagt tacttctaaa 960 ccagatttca tttcttttat tgttttatgt gccaaaccac gaagtgcatt gggcttcaat 1020 ctctgaacac tgtagaccca ttagaagact gttccgattg ttacaaattg tagtgcctga 1080 aaacactctt aagctgatgg tcttaacaaa atgaaagttc tccaaagaca aaacagaaca 1140 attattataa caaaataatt atggttgaaa tgtctgtggt tccttggaat atntgcgctc 1200 tttgtgtttt tccatcatta gtgcagttgg aatgaatgtg tataggtcag aggtcttcgt 1260 gttcacattt taaaattagg taaatgacct catctttcaa gcttgaattc atttttaatt 1320 ttaattttat tttatacaat gtgtagacag ttccctgttc tctgcattta gaagtataca 1380 caatataaat ctgttaattc tgtaagtaat ttttataatt atgatgtaac tctatcttat 1440 ccttaaaaca tttaaaataa accctttatg tgcaaaaaaa aaaaaaaaaa aaaaaaaaaa 1500 aaa 1503 <210> SEQ ID NO 138 <211> LENGTH: 174 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 138 Met Val Ser Gln Phe Leu Asp Glu Cys Asn Met Met Met Val Met Met 1 5 10 15 Thr Met Ser Leu Ile Ile Val His Leu Leu Pro Leu Gly Leu Arg Glu 20 25 30 Arg Glu Gly Leu Phe Phe Phe Leu Pro Ile Phe Pro His Ser Val Phe 35 40 45 Leu Leu Val Thr Tyr Thr Thr Cys Asn Asp Ala Met Thr Asn Ser Ala 50 55 60 Pro Lys Pro Leu Tyr Leu Gly Leu His Phe Arg Leu Met Cys Pro Asp 65 70 75 80 Leu His Ala Leu Leu Ala Phe Phe Trp Tyr Leu Asn Val Gly Ser Leu 85 90 95 Phe Gln Glu Phe Asn Ile Asn Phe Gln Lys Tyr His Gly Thr Cys Asp 100 105 110 Asn Thr Arg His Glu Ser Met Tyr Lys Ile Tyr Arg Pro Phe Ser Phe 115 120 125 Thr Cys Ser Ser Ile Ile Val Leu Cys Val Arg Ala Cys Val Met Ser 130 135 140 Gly Cys His Val Lys Leu Gln Arg Lys Ile Leu Lys Ala Asp His Pro 145 150 155 160 Phe Ala Cys Ser Ile Leu Ser Arg Met Phe Asn Val Thr Asp 165 170 <210> SEQ ID NO 139 <211> LENGTH: 1772 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 139 ggttagaatc tattgctagg gagctggtgt gatcctgtgg aggagttaaa acacggtctt 60 tttgtattgc tggaattctt gcactgattc tttctcatct gaaggaggtg ttgctgctta 120 ttttttaatt ttccatcatt tggatgggac tttttgattt tttcgtcttg tttcacttga 180 gggtatgact gtggtgtatg ttgcgtatga tcatttggct tcatttccag gtgttttcag 240 ggggccaagg ctctgtatga gttccttggt tgtggatagc ttttgtgtgg tggctttctc 300 aaatgctgct tgttgtaaca atgtattggg tgtatgagtc aacacactgt ctcctgcagg 360 gctgagagtg ctgaggtctc aggaagctta tcttgtacac tagtgctatg accttttgac 420 agcaggattt ttatttggtg gtgctatttg gttgccattc cagtaggtgg cacttaagaa 480 taaaaaccag ctcacccttg agtagtctga taatgaatag aggcaacttt cctgactggg 540 gagatccttt tggactgcac tgaggtctct tggggaaggg gtggtgaggg ggaagttgca 600 ctaacttctc aacctgggcc agcaaacatg taatccactt ccctatcaca ccctagttgc 660 attgctcatg accttcagtt cttataaaca ttgccctttg actccctgct gcagtgtggg 720 tgtggactgc aggaatgccc ctttgacagc taacaccaaa gtgggctcag tgcagagcct 780 cttataccag tccaaagcag ataatattgc acatacgtgc cttgtattgc tgggatgctg 840 ccatactgtg cagaaatggg ccctatacct tgtggaagcc ttgctatggg gatcacttaa 900 tcaggatgca gctaccatga aagcactgaa agtaacctaa aagagagtgg cagtcagcaa 960 gtacacacac atcagccccc agctggagag cctctcctgt gtctgcaaga gtagatgggg 1020 agcaggagat gaccccctgt ccatgtccat ttctgacaca tgtaccttcc cctttagcag 1080 ttggtgccat gcccatgttt ttctttgtcc taagtgggct ttggtgggct gaattcttcc 1140 ctttccctag gggcagccca tactgagtgc tggatctcca gagatgctgc agttccctag 1200 agacctgctg gcccctgtgg ttgtgaaagt caaagctggt tgtggggtac gtttgcaggg 1260 ggtctggtga tgtggcaatt caaaggctga ggttccctgg ggagggcagt gggccacaat 1320 cggtgaacaa ccaatatggc acctgctgtc tcagttcagg cctaaggggt atgcaggcac 1380 ttctgtgtga gttggtacct ggttctctat ccctggaagt tcccagattg ccaccaacag 1440 catttcctgg ggtcatgaga gcacagggac tcctcaaaaa tttggtggtc agcaaattgt 1500 gacaggggta agaggagcag agaagcccta ccctttccgt agggctatgg gtttctcagg 1560 ggttgatctc tgctgcactc ctgctgcttt ccttttctgc actacagctt cattctctgg 1620 actctctgac agatcctggt tgtcttcctt cattttttca ttcagatttt gaccattcac 1680 ctataatttt gatcttattt ctgaggagaa ctggcatctg acatccctag ttagccatct 1740 tgaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 1772 <210> SEQ ID NO 140 <211> LENGTH: 90 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 140 Met Thr Phe Ser Ser Tyr Lys His Cys Pro Leu Thr Pro Cys Cys Ser 1 5 10 15 Val Gly Val Asp Cys Arg Asn Ala Pro Leu Thr Ala Asn Thr Lys Val 20 25 30 Gly Ser Val Gln Ser Leu Leu Tyr Gln Ser Lys Ala Asp Asn Ile Ala 35 40 45 His Thr Cys Leu Val Leu Leu Gly Cys Cys His Thr Val Gln Lys Trp 50 55 60 Ala Leu Tyr Leu Val Glu Ala Leu Leu Trp Gly Ser Leu Asn Gln Asp 65 70 75 80 Ala Ala Thr Met Lys Ala Leu Lys Val Thr 85 90 <210> SEQ ID NO 141 <211> LENGTH: 1067 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 141 gaaacatgtt agttgattat acctgaaatg gattatttat ctcatcagca agtattattt 60 gaataaaatg agaaatgctt aagaaaaatt gttgctctat agtaatttgg tttcgaagaa 120 tggaatggta actatttttt cccatcgttc ttttgagaga aggaagtgtg atgactgatg 180 atcttgaaaa gcccatttct gattgcacgt tgactggaat tctttctttg tgtctgtgga 240 ctagcgatgc tgtttgtaaa atgaagattc gggactggct catatctttt tatctaacta 300 gatgtcagat cttgaaatct gtattctcga agcaattctg ccacttgatc gtattcacag 360 gggccctggt aggctccttt agaaggacca tttctgttcc tagagcttaa ctagaattca 420 ttcttcactg aaaaaaaaaa aagttactta agaaagcatt tctttcctaa tctcactcaa 480 atctgcagaa ttatttgtaa ttagtaatac aaaatctggc caaaaggaga cttgtaaata 540 gcgtaaagtg gtgtcttatg ctaaacggtg gaatgtatag gcagagaagc tctttgaagt 600 tgtcagatga gctgggctca caagcctgat tcaaacaggc tgtcggtctc ctctcacccc 660 ttaatactgt gcagcccaaa ctcctaggac tcttgaacat ctgagcagtt ttgtgctttg 720 agccactttt tgacaaaaat ggctccattt ttccacagcg tggttttctt aaaatagttt 780 aatgttttat agtctcatag tagtagtgtt gctttctaag ctataaccgt cgactttatt 840 cttctactct gaaaaatctt tacttgtttg agtgttttta atttttataa agggagcctt 900 aatggattgg ttttcataat ttaatatttt ttgtatttgc tcttgtataa ttgtttttaa 960 cggaaagtat taaagaattg agggtggaat tcttagaacc aaagttattc ttaataaaaa 1020 tcaccacatg cttggaccaa aaaaaaaaaa aaaaaaaaaa aaaaaaa 1067 <210> SEQ ID NO 142 <211> LENGTH: 79 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 142 Met Thr Asp Asp Leu Glu Lys Pro Ile Ser Asp Cys Thr Leu Thr Gly 1 5 10 15 Ile Leu Ser Leu Cys Leu Trp Thr Ser Asp Ala Val Cys Lys Met Lys 20 25 30 Ile Arg Asp Trp Leu Ile Ser Phe Tyr Leu Thr Arg Cys Gln Ile Leu 35 40 45 Lys Ser Val Phe Ser Lys Gln Phe Cys His Leu Ile Val Phe Thr Gly 50 55 60 Ala Leu Val Gly Ser Phe Arg Arg Thr Ile Ser Val Pro Arg Ala 65 70 75 <210> SEQ ID NO 143 <211> LENGTH: 1415 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1208) <400> SEQUENCE: 143 gtcaggttca ggcttttaga tgcaaataga tcttttccca tatgttttga attgctaaaa 60 cagaaagagt ggaaagaatt ttgaaacaaa caagacccct gacctactgg atcttcagtc 120 tggcctctac ctgcctcaca ggcactgctc atcccaccta ggcatggctg gatacttgag 180 ccatgctcca gccatgttgg cttctttcag ttcctccagt gccccttgct tcttcctgcc 240 acagggtctt tgcataactt tttccacttg caagtctatt ctcttttcct tcaacctctt 300 ccccatttgc ctaattaact tctctagatc ctctacatct cagttcaaac ttttctttgc 360 accagtcaca ttcgctgacc tctgtgacca ggccaacccc gtaccaaaaa tattcttccg 420 ccaagcattt ccagttatca ccttgcattt cttcctttga tgtttttgat ttatgtctac 480 atcccccacc taaccgtaag ctcctagatg aaaaagactt gttctcttta acctgctcat 540 tattccccta gcacctccaa gtatagttgg cccatcacac agcaggtgct taataaatat 600 ttgatgattt ctttaatgag tgagtgaatg aacctgttga tttcattcac cttagtctcc 660 ctcaaatttt ttccaaaaga gttactaata gtgtgaaagc tcttctgatg aagaatgcca 720 ctctgtagtt ttaactcagt aagtaagaaa gaatcataaa actcaactag ggcattgaca 780 aaatgaaagt acagtcaatg accaaaatcg tcccttttta atttttcttc taggaattta 840 agaaaagaag gcaaatttag caccagtggt ccctgtaagt gagccctagg ccatatctgg 900 atgcttttta ttttaggatc atttccaaac tagttacaat gatttttatt tgataaagtg 960 aaattcatcc caatctctag agggatactc agtctctaaa tgtttcaatg gtgccatcat 1020 cttattttta aaaagagtca cacttggacc tagatggtat gttaatgaat atataatata 1080 aggtttgaat ttttgtgtaa tttttatatt tagtttaact ttctgtttta aaaaggaagt 1140 ctggcatctt gagaattcta agaccgttta ccaaacttat tctgcattga agattggagt 1200 atgagggngt gtgggagctt ggtatcattt agtgttttat gagcaataac atgaatggta 1260 agataatttt aggaagtggt agacagattg gattcacttg gaacacagcc agaaaaatca 1320 ataaatgatt atttactaat tcagaaaaga tgatgattct aagtctttta aaatgcattt 1380 ttaaaaactg ttttccagtt cggcaaaaaa aaaaa 1415 <210> SEQ ID NO 144 <211> LENGTH: 98 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 144 Met Ala Gly Tyr Leu Ser His Ala Pro Ala Met Leu Ala Ser Phe Ser 1 5 10 15 Ser Ser Ser Ala Pro Cys Phe Phe Leu Pro Gln Gly Leu Cys Ile Thr 20 25 30 Phe Ser Thr Cys Lys Ser Ile Leu Phe Ser Phe Asn Leu Phe Pro Ile 35 40 45 Cys Leu Ile Asn Phe Ser Arg Ser Ser Thr Ser Gln Phe Lys Leu Phe 50 55 60 Phe Ala Pro Val Thr Phe Ala Asp Leu Cys Asp Gln Ala Asn Pro Val 65 70 75 80 Pro Lys Ile Phe Phe Arg Gln Ala Phe Pro Val Ile Thr Leu His Phe 85 90 95 Phe Leu <210> SEQ ID NO 145 <211> LENGTH: 1118 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 145 ggctctcctc tgggggctag aagatacttg aggcccagct tcatggggag ctcccctttg 60 ccccagacgc catgttgcaa acccttgaga aggatcctgg acagaggccc ttgcttttca 120 tctggaattc tgagtgctgc aaccttgcaa ctttggtcca gttagaattg gatcggaagc 180 tagtcaggca gcaggcgagc cccagttact cccagataac ctcctgcatt gctgtggttt 240 ctggagcttt ctgtagggtg ggcagtggga gccagggtag gtggggtagg cccgcccctg 300 cgagtgtctt cggcaccctc ccttccaccc cgccctgcgc gcggtgctct gcgccgacag 360 cccgccaacc tcttagcccc aggcccaggc cctggtggag gggagagctg ggagggctga 420 gctggtccag gtggcagagc cactcttgga gccccagctg gggtgggtcc agggcctgtg 480 ctcctgattc ccatctggag tagcctccca gagctgcttc tgggctggtg gtgtggcagt 540 gccatccttc atgtatttgg gttctctcca cagagggacc atctgtgttc tctccacccc 600 tgtctttgaa aacaaagatg ataccacgct gtacatctta gtctgcaatc tgccatcttc 660 acgtgacagt ctctcaagat ctttatatat gagagacata ttttcctttt taatatcttc 720 actgtatctc ttaggagatc tgtgattttt tttttcccaa tccgccatca tttactcaga 780 gtcagcatta aaaaaattta aaatttgtga gaggacaact atgtctgata aagcatgtca 840 tggaaggctg ggcacagcag ctcacacctg taatcccagc acttggggag accgaggcag 900 gcagatcatg aggtcaagag atcgagacca tcctggccaa catggtgaaa ccctgtctct 960 actaaaaata caaaaattat ggtggcgggt gcctgtagtt ccagctactc tggaggctga 1020 ggcaggagaa tcgcttaaac ctgggagcca ctgcactcca gcctggcagc aaagcgagac 1080 tctgtctcca aaaaaaaaaa aaaaaaaaaa aaaaaaaa 1118 <210> SEQ ID NO 146 <211> LENGTH: 143 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 146 Met Leu Gln Thr Leu Glu Lys Asp Pro Gly Gln Arg Pro Leu Leu Phe 1 5 10 15 Ile Trp Asn Ser Glu Cys Cys Asn Leu Ala Thr Leu Val Gln Leu Glu 20 25 30 Leu Asp Arg Lys Leu Val Arg Gln Gln Ala Ser Pro Ser Tyr Ser Gln 35 40 45 Ile Thr Ser Cys Ile Ala Val Val Ser Gly Ala Phe Cys Arg Val Gly 50 55 60 Ser Gly Ser Gln Gly Arg Trp Gly Arg Pro Ala Pro Ala Ser Val Phe 65 70 75 80 Gly Thr Leu Pro Ser Thr Pro Pro Cys Ala Arg Cys Ser Ala Pro Thr 85 90 95 Ala Arg Gln Pro Leu Ser Pro Arg Pro Arg Pro Trp Trp Arg Gly Glu 100 105 110 Leu Gly Gly Leu Ser Trp Ser Arg Trp Gln Ser His Ser Trp Ser Pro 115 120 125 Ser Trp Gly Gly Ser Arg Ala Cys Ala Pro Asp Ser His Leu Glu 130 135 140 <210> SEQ ID NO 147 <211> LENGTH: 1582 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 147 ccagctcctc cgggtgcagg gtccctcctg ctgaccagcc tccagctctt cccagttctg 60 ggctccgcag cgagcggctt gggggcacta cctgacacag gagaccatgt ctgggcagag 120 ggtggctgca ggtggagtct gtggcgtgtg gcgcacaccc aggggctccc ccgatgctgg 180 ttactatctg ggctatggtg gccacagctg tcttgcccct cctcacggcc gtgctgggtg 240 ttaccgtggt cacccgcagg gacacggagg ggccaggcag agcagcccta gttcacctca 300 ccgggagccc ccgccagaag gtgggcacct ctgggaggga gggactgcca ggccttgggg 360 cttcctgtgc tgagtcagag ctggaacggg agacgcagga gccccgcagc tgcgggaggt 420 gcagatttgg ggctgccagg tggcgccagg tccccttggc cagcccccag cgcccctttc 480 ttctgtcccc agggcctcgg cttcacagga tggggctgcc agtgtcctgg gcccctcctg 540 ccctctgggt tctagggtgc tgcgccctgc tcctctcgct gtgggcgctg tgcacagcct 600 gccgcagccg gaggacgctg tagcccccag gaagagggcg cggaggcagc gggcgaggct 660 gcagggcagt gcgacggcgg cggaagcgca agtcggacac cagactgcac gagctgcacc 720 ggggcccgcg cagcagcaag ggccctgcgg cctgccagca tggatctcct gcgcccacac 780 tggctggagg tgtccaggga catcacggga ccgcaggcag cccccctctg ccttcccaca 840 ccaggagctg ccccgggctc tgccggcagc tgcagccacc gcaggtgcgc tggcctcgag 900 gccacctatt ccaacgtggg gctggcggcc cttcccgggg tcacctggcg gccagccctg 960 tggtggccga gtatgcccgc gtccagaagc gcaaagggac ccatcgcatt ccccaagagc 1020 cacagcaggg gaagactgag gtgaccccgg ccgctcaggt ggacgtcctg tactccaggg 1080 tctgcaagcc taaaaggagg gacccaggac ccaccacaga cccgctggac cccaagggcc 1140 agggagcgat tctggcctgg cgggtgacct ggcctaccag accctcccgc tcagggccct 1200 ggatgtggac agcggccccc tggaaaacgt gtatgagagc atccgggagc tgggggaccc 1260 tgctggcagg agcagcacgt gcggggctgg gacgccccct gcttccagct gccccagcct 1320 agggaggggc tggagacccc tccctgcctc cctgccctga acactcaagg acctgtgctc 1380 cttcctccag agtgaggccc gtcccccgcc ccgccccgcc tcacagctga cagcgccagt 1440 cccaggtccc cggctgccag cccgtgaggt ccgtgaggtc ctggccgctc tgacagccgc 1500 ggcctccccg ggctccagag aaggcccgcg tctaaataaa gcgccagcgc aggatgaaaa 1560 aaaaaaaaaa aaaaaaaaaa aa 1582 <210> SEQ ID NO 148 <211> LENGTH: 149 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 148 Met Leu Val Thr Ile Trp Ala Met Val Ala Thr Ala Val Leu Pro Leu 1 5 10 15 Leu Thr Ala Val Leu Gly Val Thr Val Val Thr Arg Arg Asp Thr Glu 20 25 30 Gly Pro Gly Arg Ala Ala Leu Val His Leu Thr Gly Ser Pro Arg Gln 35 40 45 Lys Val Gly Thr Ser Gly Arg Glu Gly Leu Pro Gly Leu Gly Ala Ser 50 55 60 Cys Ala Glu Ser Glu Leu Glu Arg Glu Thr Gln Glu Pro Arg Ser Cys 65 70 75 80 Gly Arg Cys Arg Phe Gly Ala Ala Arg Trp Arg Gln Val Pro Leu Ala 85 90 95 Ser Pro Gln Arg Pro Phe Leu Leu Ser Pro Gly Pro Arg Leu His Arg 100 105 110 Met Gly Leu Pro Val Ser Trp Ala Pro Pro Ala Leu Trp Val Leu Gly 115 120 125 Cys Cys Ala Leu Leu Leu Ser Leu Trp Ala Leu Cys Thr Ala Cys Arg 130 135 140 Ser Arg Arg Thr Leu 145 <210> SEQ ID NO 149 <211> LENGTH: 1172 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 149 tttcctgggg agagctaccc gccagcttgg gctgccgtgg gcccctggct gaacaacgtc 60 ctgtgtctgg caggtggctg aggtcctgtg ctctggtgtg tgggtgattg ggcagggcct 120 gagctggaca ggggagctcc tagtagggga ggggagggga tgctgggatc taggtgacat 180 gcctgtccct gtctgctccc gtctgggctg ccagacgtcc ttctcttccc ggataagaag 240 cagaggacct tccagccacc cgcgacaggc cacaagcgtt ccacgagcga aggcgcctgg 300 ccacagctgc cctctggcct ctccatgatg aggtgcctcc acaacttcct gacagatggg 360 gtcctgcgga gggggcgttc actgaagact tccagggcct acgggcagag gtggagacca 420 tctccaagga actggagctt ttggacagag agctgtgcca gctgctgctg gagggcctgg 480 agggggtgct gcgggaccag ctggccctgc gagcccttgg acgacgcgct ggagcagggc 540 cagagccttg ggccggtgga gcccctggac ggtccagcag gtgctgtcct ggagtgcctg 600 gtgttgtcct ccggaatgct ggtgccggaa ctcgctatcc ctgttgtcta cctgctgggg 660 gcactgacca tgctgagtga aacgcagcac aagctgctgg cggaggcgct ggagtcgcag 720 accctgttgg ggccgctcga gctggtgggc agcctcttgg agcagagtgc cccgtggcag 780 gagcgcagca ccatgtccct gccccccggg ctcctgggga acagctgggg cgaaggagca 840 ccggcctggg tcttgctgga cgagtgtggc ctagagctgg gggaggacac tccccacgtg 900 tgctgggagc cgcaggccca gggccgcatg tgtgcactct acgcctccct ggcactgcta 960 tcaggactga gccaggagcc ccactagcct gtgcccgggc atggcctggc agctctccag 1020 cagggcagag tgtttgccca ccagctgcta gccctaggaa ggccaggagc ccagtagcca 1080 tgtggccagt ctaccatggg gcccaggagt tggggaaaca caataaaggt ggcatacgaa 1140 ggaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 1172 <210> SEQ ID NO 150 <211> LENGTH: 220 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 150 Met Met Arg Cys Leu His Asn Phe Leu Thr Asp Gly Val Leu Arg Arg 1 5 10 15 Gly Arg Ser Leu Lys Thr Ser Arg Ala Tyr Gly Gln Arg Trp Arg Pro 20 25 30 Ser Pro Arg Asn Trp Ser Phe Trp Thr Glu Ser Cys Ala Ser Cys Cys 35 40 45 Trp Arg Ala Trp Arg Gly Cys Cys Gly Thr Ser Trp Pro Cys Glu Pro 50 55 60 Leu Asp Asp Ala Leu Glu Gln Gly Gln Ser Leu Gly Pro Val Glu Pro 65 70 75 80 Leu Asp Gly Pro Ala Gly Ala Val Leu Glu Cys Leu Val Leu Ser Ser 85 90 95 Gly Met Leu Val Pro Glu Leu Ala Ile Pro Val Val Tyr Leu Leu Gly 100 105 110 Ala Leu Thr Met Leu Ser Glu Thr Gln His Lys Leu Leu Ala Glu Ala 115 120 125 Leu Glu Ser Gln Thr Leu Leu Gly Pro Leu Glu Leu Val Gly Ser Leu 130 135 140 Leu Glu Gln Ser Ala Pro Trp Gln Glu Arg Ser Thr Met Ser Leu Pro 145 150 155 160 Pro Gly Leu Leu Gly Asn Ser Trp Gly Glu Gly Ala Pro Ala Trp Val 165 170 175 Leu Leu Asp Glu Cys Gly Leu Glu Leu Gly Glu Asp Thr Pro His Val 180 185 190 Cys Trp Glu Pro Gln Ala Gln Gly Arg Met Cys Ala Leu Tyr Ala Ser 195 200 205 Leu Ala Leu Leu Ser Gly Leu Ser Gln Glu Pro His 210 215 220 <210> SEQ ID NO 151 <211> LENGTH: 1111 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 151 attgaattct gccccacatg ttgacagtag agttggaact ggattcttgg gattacttat 60 ctaaaaaact ggagcatcag gtccatttct gttctgctgg tttggaatct tttccgtaat 120 gctatttatt gccaacaatg gcctctcttt gtgtccatat atgccttaca ccgtgctgac 180 ctgggtatca tccatgtgct ctgaagcatc caactttact ttgcaggtgc atcaatgtag 240 tcctgtccct gaactgagta accgtgttcc tgaaaagtac actagggaaa ttcacctgct 300 tgcttgtctt tgtattggca tggcacttgt gattgcacca tggagcatgc tcagagctat 360 taaattggtc tcccatctcc caccaggata tgaaaggtcc atatgggagg ccacgtaatc 420 acttattaca gtggttacat aatacactgg ctcactgcag actctcttgt tttttgatac 480 agtttcgtgc tggcttcatt tgccaattgt gttgtttagt tcggaagtaa gagggtcttg 540 agattgaggg gtagggaggg ctacactgac tgatccgtgg cttaagacag gagattatct 600 ctgtactcca gtggcatctc cttagccaag atgtgaaata aaaatcatag ttcgcctcat 660 ttaaaaattc taataaagca ctcaaacttt gaaaagcttt tacttttccc tcctactaaa 720 aaaaatgtat gtacctcata gccctgtgtc atttagtgtt cagcactttt gggaacatca 780 gttggtgaac tttaaaattt gctgtctact cactgggcac ggtggctcac acctgtaatc 840 ccagcacttt gggaggctga ggcaggtgga tcacctgagg tcaggagttt gagaccagcc 900 tgaccaacat ggtgaaaccc cgtctctact aaaaatgcag aaattaggtg ggcgcctgta 960 atcccagcta cttgggaggc tgaggcgaga taatcgcttg aacctgggag gcagaggttg 1020 cagtgagccg agattgcacc actgtcgccc accctgggtg ataagagtga aactccttct 1080 caaaaaaaaa aaaaaaaaaa aaaaaaaaaa a 1111 <210> SEQ ID NO 152 <211> LENGTH: 99 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 152 Met Leu Phe Ile Ala Asn Asn Gly Leu Ser Leu Cys Pro Tyr Met Pro 1 5 10 15 Tyr Thr Val Leu Thr Trp Val Ser Ser Met Cys Ser Glu Ala Ser Asn 20 25 30 Phe Thr Leu Gln Val His Gln Cys Ser Pro Val Pro Glu Leu Ser Asn 35 40 45 Arg Val Pro Glu Lys Tyr Thr Arg Glu Ile His Leu Leu Ala Cys Leu 50 55 60 Cys Ile Gly Met Ala Leu Val Ile Ala Pro Trp Ser Met Leu Arg Ala 65 70 75 80 Ile Lys Leu Val Ser His Leu Pro Pro Gly Tyr Glu Arg Ser Ile Trp 85 90 95 Glu Ala Thr <210> SEQ ID NO 153 <211> LENGTH: 551 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 153 ggctggcgtt tcccacattt ctctgtggga gggtccttga gaggacacag ggatgaaatg 60 gtgactctgt ccagcaccct tggacagaga agcctatgcc ggagccacct ctcactacag 120 gtcctgagct tggtgctgag gacgcctgga ggaatcacag agcccatctg gaacagccca 180 tctcctggct gggttggatc agcctctggt ttcttctcag agcactgaga aggtctggct 240 caaccacctc caagattcat cttgttctgt ggacacagca tctagtgaca caagacaaga 300 gagcaccaaa actctctagg agcacaggaa gtccttcagc tttcaggaat cagaagaggt 360 gtcacagctc tgaagaataa ggacttccac aagcccagga gatgagaagg ggtggaagtt 420 ggaggggcgg gactgggtgg agtggacatt ccaggagctg ggtgaggtaa aaacacggag 480 gcaggaaaat gcggagtgct ttggaaacca taaaaaaaaa aaaaaaaaaa aaaaaaaaaa 540 aaaaaaaaaa a 551 <210> SEQ ID NO 154 <211> LENGTH: 94 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 154 Met Pro Glu Pro Pro Leu Thr Thr Gly Pro Glu Leu Gly Ala Glu Asp 1 5 10 15 Ala Trp Arg Asn His Arg Ala His Leu Glu Gln Pro Ile Ser Trp Leu 20 25 30 Gly Trp Ile Ser Leu Trp Phe Leu Leu Arg Ala Leu Arg Arg Ser Gly 35 40 45 Ser Thr Thr Ser Lys Ile His Leu Val Leu Trp Thr Gln His Leu Val 50 55 60 Thr Gln Asp Lys Arg Ala Pro Lys Leu Ser Arg Ser Thr Gly Ser Pro 65 70 75 80 Ser Ala Phe Arg Asn Gln Lys Arg Cys His Ser Ser Glu Glu 85 90 <210> SEQ ID NO 155 <211> LENGTH: 888 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 155 gccgccgccc aggaagggga tgcggaaacc cctggctcgg tggagcggag aggcaggcgg 60 ggtgaggggc gttgccaggc aaagggcgag cgccgtggct ggggagccga ggacggcatg 120 tcccaggccc cgggagcaca gccgagccca cccaccgtgt accacgaacg gcagcgcctg 180 gagctgtgtg ctgtccacgc cctcaacaac gttctgcagc agcagctctt tagccaggag 240 gctgccgatg agatctgcaa gaggttggcc ccagactccc ggctgaaccc tcatcgcagc 300 ctcctgggca ccggcaacta tgatgtcaat gtgatcatgg ccgctctgca ggggctgggc 360 ctggccgccg tgtggtggga caggaggagg cccctgtccc agctggccct gccccaggta 420 ctggggctga tcctgaacct gccctcgccc gtgtcgctgg ggctgctgtc actgccgctg 480 cgccggcggc actgggtggc cctgcgccag gtggacggtg tctactacaa cctggactcc 540 aagctgcggg cgcccgaggc cctgggggat gaggacggag tcagggcctt cctggcggct 600 gcgctggccc agggcctgtg cgaggtgctg ctggtagtga ccaaggaggt ggaggagaag 660 ggcagctggc tgcggacaga ctgaccatgg ctgaccatcg gcgcccacag cgcagtccct 720 gcgcatcccc ctccggtgcg cacactgcat gcctgggaaa ggccagcact tcatggaccc 780 tggggaggcc ccgccccctc cccacacccc tgctccccac tgccgctgct gcctcaataa 840 atctgctgat ttgctgccaa aaaaaaaaaa aaaaaaaaaa aaaaaaaa 888 <210> SEQ ID NO 156 <211> LENGTH: 188 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 156 Met Ser Gln Ala Pro Gly Ala Gln Pro Ser Pro Pro Thr Val Tyr His 1 5 10 15 Glu Arg Gln Arg Leu Glu Leu Cys Ala Val His Ala Leu Asn Asn Val 20 25 30 Leu Gln Gln Gln Leu Phe Ser Gln Glu Ala Ala Asp Glu Ile Cys Lys 35 40 45 Arg Leu Ala Pro Asp Ser Arg Leu Asn Pro His Arg Ser Leu Leu Gly 50 55 60 Thr Gly Asn Tyr Asp Val Asn Val Ile Met Ala Ala Leu Gln Gly Leu 65 70 75 80 Gly Leu Ala Ala Val Trp Trp Asp Arg Arg Arg Pro Leu Ser Gln Leu 85 90 95 Ala Leu Pro Gln Val Leu Gly Leu Ile Leu Asn Leu Pro Ser Pro Val 100 105 110 Ser Leu Gly Leu Leu Ser Leu Pro Leu Arg Arg Arg His Trp Val Ala 115 120 125 Leu Arg Gln Val Asp Gly Val Tyr Tyr Asn Leu Asp Ser Lys Leu Arg 130 135 140 Ala Pro Glu Ala Leu Gly Asp Glu Asp Gly Val Arg Ala Phe Leu Ala 145 150 155 160 Ala Ala Leu Ala Gln Gly Leu Cys Glu Val Leu Leu Val Val Thr Lys 165 170 175 Glu Val Glu Glu Lys Gly Ser Trp Leu Arg Thr Asp 180 185 <210> SEQ ID NO 157 <211> LENGTH: 659 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 157 gaaacactga atatttcaac agcagaaatt gaatgggggg attgatagcg ctggcgaggg 60 aagcagctgg aaagagacag atggcaccct gagacagccc agaggtgaat aggaccccca 120 ggctgcaggg ataaagctca gtggtggtgt tacctcaccg gggaccaggg tcacacagca 180 aagctggaac aacagaggcg tgttgtgggg gagcctcaga ggggacaaaa cctctgcctg 240 agatcccacc ccaggtgggc atgggggcca ctgaggttgg ggatgaaaat gccggtaccg 300 tcagtgcaca gccctgttcc agacagtgct gcctggaaga tttctgggct ctcctgaggc 360 gccaccccgc acctgagcca cctccttgga ctcctgtcct ctaccccttg aggacctccc 420 tcccttctac cctagctgtc ttcttgaact tgggactctc ctttcccaag acttccatca 480 ctagctcctg gagggactgg actttgcatc ttcccttcgc gtggagcctc agtgtgagag 540 gccctgccaa tgcgtgcatg tcagaggtgg tggggaccac atcagaagaa gaggggggtg 600 atgaaattaa caaataaaaa gtatggggaa acaaaaaaaa aaaaaaaaaa aaaaaaaaa 659 <210> SEQ ID NO 158 <211> LENGTH: 118 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 158 Met Gly Ala Thr Glu Val Gly Asp Glu Asn Ala Gly Thr Val Ser Ala 1 5 10 15 Gln Pro Cys Ser Arg Gln Cys Cys Leu Glu Asp Phe Trp Ala Leu Leu 20 25 30 Arg Arg His Pro Ala Pro Glu Pro Pro Pro Trp Thr Pro Val Leu Tyr 35 40 45 Pro Leu Arg Thr Ser Leu Pro Ser Thr Leu Ala Val Phe Leu Asn Leu 50 55 60 Gly Leu Ser Phe Pro Lys Thr Ser Ile Thr Ser Ser Trp Arg Asp Trp 65 70 75 80 Thr Leu His Leu Pro Phe Ala Trp Ser Leu Ser Val Arg Gly Pro Ala 85 90 95 Asn Ala Cys Met Ser Glu Val Val Gly Thr Thr Ser Glu Glu Glu Gly 100 105 110 Gly Asp Glu Ile Asn Lys 115 <210> SEQ ID NO 159 <211> LENGTH: 550 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 159 ccttgagtct ccgggccgcc ttgccatggc tgcccgtggt gtcatcgctc cagttggcga 60 gagtttgcgc tacgctgagt acttgcagcc ctcggccaaa cggccagacg ccgacgtcga 120 ccagcagaga ctggtaagaa gtttgatagc tgtaggcctg ggtgttgcag ctcttgcatt 180 tgcaggtcgc tacgcatttc ggatctggaa acctctagaa caagttatca cagaaactgc 240 aaagaagatt tcaactccta gcttttcatc ctactataaa ggaggatttg aacagaaaat 300 gagtaggcga gaagctggtc ttattttagg tgtaagccca tctgctggca aggctaagat 360 tagaacagct cataggagag tcatgatttt gaatcaccca gataaaggtg gatctcctta 420 cgtagcagcc aaaataaatg aagcaaaaga cttgctagaa acaaccacca aacattgatg 480 cttaaggacc acactgaagg aaaaaaaaag aggggactcc aaaaaaaaaa aaaaaaaaaa 540 aaaaaaaaaa 550 <210> SEQ ID NO 160 <211> LENGTH: 150 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 160 Met Ala Ala Arg Gly Val Ile Ala Pro Val Gly Glu Ser Leu Arg Tyr 1 5 10 15 Ala Glu Tyr Leu Gln Pro Ser Ala Lys Arg Pro Asp Ala Asp Val Asp 20 25 30 Gln Gln Arg Leu Val Arg Ser Leu Ile Ala Val Gly Leu Gly Val Ala 35 40 45 Ala Leu Ala Phe Ala Gly Arg Tyr Ala Phe Arg Ile Trp Lys Pro Leu 50 55 60 Glu Gln Val Ile Thr Glu Thr Ala Lys Lys Ile Ser Thr Pro Ser Phe 65 70 75 80 Ser Ser Tyr Tyr Lys Gly Gly Phe Glu Gln Lys Met Ser Arg Arg Glu 85 90 95 Ala Gly Leu Ile Leu Gly Val Ser Pro Ser Ala Gly Lys Ala Lys Ile 100 105 110 Arg Thr Ala His Arg Arg Val Met Ile Leu Asn His Pro Asp Lys Gly 115 120 125 Gly Ser Pro Tyr Val Ala Ala Lys Ile Asn Glu Ala Lys Asp Leu Leu 130 135 140 Glu Thr Thr Thr Lys His 145 150 <210> SEQ ID NO 161 <211> LENGTH: 622 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 161 ctcacctgtg ctgccacttc ctagtgcaca cctcacggct catcctcaag ctggaagata 60 cctctctggc cccggcacat gtcacccctg cactcctgcc ttcccgtggg cacttccaca 120 tcctctgggc ctctggcagt tcccagggac tgttttcacc tctgctgtct ctggggtcag 180 ctgctgctca tcagctgccc gctagcatgt ggccaggggt gcagggtggc ggggggtcag 240 cagcatgtcc ctgggcaggc cctgggcacc ctgtctcccc tggtctcact gctgacctgg 300 gctggtccca gcctggattg gcctcatcca ggatctttgg tcaccccacg ctgccccatc 360 ttgcctgctg ttccagttct ggtcaagggc cttgggggct ggccccccac caggccttct 420 agagcagcac cagtctcagg gccctgggac cagctgccct acttcccagg tttgtagcca 480 ggagaagggg gcatcacaga gctgatggtc caataagggg ggtgtgagcc ccgcagggac 540 tggcccgcac ctgccttgga tgttttcagc aattaaactt ttttaagctg acaaaaaaaa 600 aaaaaaaaaa aaaaaaaaaa aa 622 <210> SEQ ID NO 162 <211> LENGTH: 132 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 162 Met Ser Pro Leu His Ser Cys Leu Pro Val Gly Thr Ser Thr Ser Ser 1 5 10 15 Gly Pro Leu Ala Val Pro Arg Asp Cys Phe His Leu Cys Cys Leu Trp 20 25 30 Gly Gln Leu Leu Leu Ile Ser Cys Pro Leu Ala Cys Gly Gln Gly Cys 35 40 45 Arg Val Ala Gly Gly Gln Gln His Val Pro Gly Gln Ala Leu Gly Thr 50 55 60 Leu Ser Pro Leu Val Ser Leu Leu Thr Trp Ala Gly Pro Ser Leu Asp 65 70 75 80 Trp Pro His Pro Gly Ser Leu Val Thr Pro Arg Cys Pro Ile Leu Pro 85 90 95 Ala Val Pro Val Leu Val Lys Gly Leu Gly Gly Trp Pro Pro Thr Arg 100 105 110 Pro Ser Arg Ala Ala Pro Val Ser Gly Pro Trp Asp Gln Leu Pro Tyr 115 120 125 Phe Pro Gly Leu 130 <210> SEQ ID NO 163 <211> LENGTH: 596 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 163 ctcgcttctc tgcattacac gccggtcagg attcgcgacc cgacatggag cgtccccgca 60 gtccccaatg ctcggccccg gcctctgcct cagcttcggt taccctggcg cagctcctgc 120 agctggtcca gcagggccag gaactcccgg gcctggagaa acgccacatc gcggcgatcc 180 acggcgaacc cacagcgtcc cggctgccgc ggaggcccaa gccctgggag gccgcggctt 240 tggctgagtc ccttccccct ccgaccctca ggataggaac ggccccggcg gagcctggct 300 tggttgaggc agcgactgcg ccttcttcat ggcatacagt gggcccctga ggttccaggt 360 cctttgcggc ggcgatctgg agggcgtggc tacaggaccc gggatgccat tcagttactc 420 atcttttatg ctttcgtcct gacctgtctc aactagactt gctcctgcaa ccaccatggg 480 ggttttgcat ttacatttgt ggaccatgtt acagttaaga aaaatcctgt ttcagtcctt 540 atatgtaata aaatgtttta tgatggaaaa aaaaaaaaaa aaaaaaaaaa aaaaaa 596 <210> SEQ ID NO 164 <211> LENGTH: 101 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 164 Met Glu Arg Pro Arg Ser Pro Gln Cys Ser Ala Pro Ala Ser Ala Ser 1 5 10 15 Ala Ser Val Thr Leu Ala Gln Leu Leu Gln Leu Val Gln Gln Gly Gln 20 25 30 Glu Leu Pro Gly Leu Glu Lys Arg His Ile Ala Ala Ile His Gly Glu 35 40 45 Pro Thr Ala Ser Arg Leu Pro Arg Arg Pro Lys Pro Trp Glu Ala Ala 50 55 60 Ala Leu Ala Glu Ser Leu Pro Pro Pro Thr Leu Arg Ile Gly Thr Ala 65 70 75 80 Pro Ala Glu Pro Gly Leu Val Glu Ala Ala Thr Ala Pro Ser Ser Trp 85 90 95 His Thr Val Gly Pro 100 <210> SEQ ID NO 165 <211> LENGTH: 670 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 165 cttagaaagc ggcggtgagg tcagcttcac attctcagga actctccttc tttgggtctg 60 gctgaagttg aggatctctt actctctagg ccacggaatt aacccgagca ggcatggagg 120 cctctgctct cacctcatca gcagtgacca gtgtggccaa agtggtcagg gtggcctctg 180 gctctgccgt agttttgccc ctggccagga ttgctacagt tgtgattgga ggagttgtgg 240 ctgtgcccat ggtgctcagt gccatgggct tcactgcggg gggaatcgcc tcgtcctcca 300 tagcagccaa gatgatgtcc gcggcggcca ttgccaatgg gggtggagtt gcctcgggca 360 gccttgtggc tactctgcag tcactgggag caactggact ctccggattg accaagttca 420 tcctgggctc cattgggtct gccattgcgg ctgtcattgc gaggttctac tagctccctg 480 cccctcgccc tgcagagaag agaaccatgc caggggagaa ggcacccagc catcctgacc 540 cagcgaggag ccaactatcc caaatatacc tggggtgaaa tataccaaat tctgcatctc 600 cagaggaaaa taagaaataa agatgaattg ttgcaactat aaaaaaaaaa aaaaaaaaaa 660 aaaaaaaaaa 670 <210> SEQ ID NO 166 <211> LENGTH: 119 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 166 Met Glu Ala Ser Ala Leu Thr Ser Ser Ala Val Thr Ser Val Ala Lys 1 5 10 15 Val Val Arg Val Ala Ser Gly Ser Ala Val Val Leu Pro Leu Ala Arg 20 25 30 Ile Ala Thr Val Val Ile Gly Gly Val Val Ala Val Pro Met Val Leu 35 40 45 Ser Ala Met Gly Phe Thr Ala Gly Gly Ile Ala Ser Ser Ser Ile Ala 50 55 60 Ala Lys Met Met Ser Ala Ala Ala Ile Ala Asn Gly Gly Gly Val Ala 65 70 75 80 Ser Gly Ser Leu Val Ala Thr Leu Gln Ser Leu Gly Ala Thr Gly Leu 85 90 95 Ser Gly Leu Thr Lys Phe Ile Leu Gly Ser Ile Gly Ser Ala Ile Ala 100 105 110 Ala Val Ile Ala Arg Phe Tyr 115 <210> SEQ ID NO 167 <211> LENGTH: 850 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 167 caaacttaca cagtgctttg ggaattccaa agtactcagt ggagagaggt gtttcaggag 60 ccgtagagcc agatcgtcat catgtctgca ttgtggctgc tgctgggcct ccttgccctg 120 atggacttgt ctgaaagcag caactgggga tgctatggaa acatccaaag cctggacacc 180 cctggagcat cttgtgggat tggaagacgt cacggcctga actactgtgg agttcgtgct 240 tctgaaaggc tggctgaaat agacatgcca tacctcctga aatatcaacc catgatgcaa 300 accattggcc aaaagtactg catggatcct gccgtgatcg ctggtgtctt gtccaggaag 360 tctcccggtg acaaaattct ggtcaacatg ggcgatagga ctagcatggt gcaggaccct 420 ggctctcaag ctcccacatc ctggattagt gagtctcagg tttcccagac aactgaagtt 480 ctgactacta gaatcaaaga aatccagagg aggtttccaa cctggacccc tgaccagtac 540 ctgagaggtg gactctgtgc ctacagtggg ggtgctggct atgtccgaag cagccaggac 600 ctgagctgtg acttctgcaa tgatgtcctt gcacgagcca agtacctcaa gagacatggc 660 ttctaacatc tcagatgaaa cccaagacca tgatcacata tgcagcctca aatgttacac 720 agataaaact agccaagggc acctgtaact gggaatctga gtttgaccta aaagtcatta 780 aaataacatg aatcacatta aaggaagaat tttgacctgc aaaaaaaaaa aaaaaaaaaa 840 aaaaaaaaaa 850 <210> SEQ ID NO 168 <211> LENGTH: 194 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 168 Met Ser Ala Leu Trp Leu Leu Leu Gly Leu Leu Ala Leu Met Asp Leu 1 5 10 15 Ser Glu Ser Ser Asn Trp Gly Cys Tyr Gly Asn Ile Gln Ser Leu Asp 20 25 30 Thr Pro Gly Ala Ser Cys Gly Ile Gly Arg Arg His Gly Leu Asn Tyr 35 40 45 Cys Gly Val Arg Ala Ser Glu Arg Leu Ala Glu Ile Asp Met Pro Tyr 50 55 60 Leu Leu Lys Tyr Gln Pro Met Met Gln Thr Ile Gly Gln Lys Tyr Cys 65 70 75 80 Met Asp Pro Ala Val Ile Ala Gly Val Leu Ser Arg Lys Ser Pro Gly 85 90 95 Asp Lys Ile Leu Val Asn Met Gly Asp Arg Thr Ser Met Val Gln Asp 100 105 110 Pro Gly Ser Gln Ala Pro Thr Ser Trp Ile Ser Glu Ser Gln Val Ser 115 120 125 Gln Thr Thr Glu Val Leu Thr Thr Arg Ile Lys Glu Ile Gln Arg Arg 130 135 140 Phe Pro Thr Trp Thr Pro Asp Gln Tyr Leu Arg Gly Gly Leu Cys Ala 145 150 155 160 Tyr Ser Gly Gly Ala Gly Tyr Val Arg Ser Ser Gln Asp Leu Ser Cys 165 170 175 Asp Phe Cys Asn Asp Val Leu Ala Arg Ala Lys Tyr Leu Lys Arg His 180 185 190 Gly Phe <210> SEQ ID NO 169 <211> LENGTH: 494 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 169 gccagtgctt ctaattttga cttagtttca tacagtaaag cctaaatgtg aaacgcacac 60 gctggaagat attgttccta tcaatatttt gctttttata acaagggttt gttcatattg 120 atgccatttt tgcaggattt cttcgtgatt tctgtccata tgaaaatgct gacattaaac 180 attaacacat ggagaccgtg ccctgtggcc ctgccgtggc tgccagcatg gtctgtgttt 240 ccttgtggat tcacctgtgg ccctgctgtg gccaccagca tggtctgtgt cctcgtggat 300 tcactgcagc tgtcggatgc gagtttctgt cataatcatt tgtttcctga tacaattgtt 360 cttattcttt tccaaaactg taaaataatc tcctccctca aatgcaaagg ttgtttttgt 420 tctgtttctg ttttctttga aataaaatta taacgttaaa agacaaaaaa aaaaaaaaaa 480 aaaaaaaaaa aaaa 494 <210> SEQ ID NO 170 <211> LENGTH: 110 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 170 Met Pro Phe Leu Gln Asp Phe Phe Val Ile Ser Val His Met Lys Met 1 5 10 15 Leu Thr Leu Asn Ile Asn Thr Trp Arg Pro Cys Pro Val Ala Leu Pro 20 25 30 Trp Leu Pro Ala Trp Ser Val Phe Pro Cys Gly Phe Thr Cys Gly Pro 35 40 45 Ala Val Ala Thr Ser Met Val Cys Val Leu Val Asp Ser Leu Gln Leu 50 55 60 Ser Asp Ala Ser Phe Cys His Asn His Leu Phe Pro Asp Thr Ile Val 65 70 75 80 Leu Ile Leu Phe Gln Asn Cys Lys Ile Ile Ser Ser Leu Lys Cys Lys 85 90 95 Gly Cys Phe Cys Ser Val Ser Val Phe Phe Glu Ile Lys Leu 100 105 110 <210> SEQ ID NO 171 <211> LENGTH: 2262 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 171 gtgctcagtg ttcacgctat atcccttggg caatgtgggg ttggatgggg cccccacttc 60 cattcccatg gaaggaggcc aggtccccag ccacctccca ctcagccatg cacgcacttg 120 ctgggctggc ctcctgggaa acacaggtga ctcgaatgaa ctctgcattt tcaacgtgcc 180 ttctactgct tcaggacctg ggggtccccc tgaccctcac tggcttgccc ccagccctgg 240 gcctggcccc acctgtcctg gagcccagag cccctggcct ggagctgcct ctctggggtg 300 ggtctcaggc cccacccctc cctcttttga gttcagtgcc ttgctcagcc cctcccatgt 360 atctcagcgt cttcagacct ctgacagagc gacgatgtag ggtctcccgg ggcccaaggt 420 ggtctcaggg tcaggggtgg gatttgcagg gaactcgggg agcccacggg ttgcgccacc 480 tctgccctgg cagctgaagc ctgggagagt ccctgcgtgg tgtaattggc ctcagcccgc 540 tttctctgtg ccgtcgcacc tcagtgtttc tcatagcttg tccccacgtg tcactttcca 600 tccacgggaa aaacaaatgc cccttctcca tctatcattg cgacttcctc ccaggaggcc 660 tctcaggttg ggtagagcag gggcctgcag tggtcaggcc aagagcaagg aagacctggc 720 tgccccactg tggctgaaaa ctcaaaacat ctggaactac ccttctccaa ttacgttccc 780 tcttgcttaa agacaaagct aattaaatca tcctgccacc cgaggctcca aaccaaatct 840 tggacgcaaa ttaatgagtt tgataagccc aggttgattg atgagacagt ctggaaccgc 900 caagccatgg agtcggtggc cgtgttcccg gccctggagg gaactggcca gcagtgacca 960 catcgatgat gccgagtggg gaccctcacc actgcggtgg tcaagctgct tggctcctca 1020 gtgtcctcgt gctgtaagtc agatgaggtc accttcctct ccatcgatgc caggcttctg 1080 ccgctgacgg ccaatggggc ttggggccag gggcagagaa ccccaacagc aagagagccc 1140 caggtgatgc tggctctcca cgtgcatccg gcacgtttca ctgcagccat catcaacttg 1200 gcaaagtagg caagctcagc ttgtggtttc cattttgcag atgggccccc ggggtcagtg 1260 atgggaagag cagaagagga tgccagccca gcctggccca ggagcaggtg tcgttgtgga 1320 ggaaagctta aactcaacag cctctaccca acatctgcca cctgcatggc cccagatgcc 1380 cccggtgcag gccaggtcaa ggtgggagta aactttcttt gcctccctcc ccacagaagc 1440 accagaccca cttgagcccc agagcctcat gccagcagct cctggctgtt cctcacctga 1500 ggctagagca gcagctgcca gcttatagat ggggcggctg gcaggtgata gaatgggaag 1560 cattggtggg tggtggaggt gggcagtggc accatgacgg gcccctagcc aaacagctgt 1620 cctcaatacg gggcagggag cagccttggc aacaggcaaa ggccagagtc agagtggtgg 1680 ggaggacagg ggctgctgcc ccgctcctgg aaagccactg cagaggggca gtggctggca 1740 gtgccaggcc tgggggaagt ggaagcgtcc tgtctggggg cagattccca agcaaggtga 1800 cccatggtta agggccactg gaaagctgga gagagcttgg gatcccttcc acctggggcc 1860 aatggtgttg attgcagact ggaggggtaa cctccgctga gggtcattat gtgccaggca 1920 tggcattggg tactttctgc attgggacca ggcagccggg cctgccattt gaggcagcga 1980 gcctccgtga cctgtcctcc ctcatttgta aagtggggta acagctatgt cactggccag 2040 ttgtggggat taaagtgctg agctatagtg cccagcccaa aatgctcaat aaagctattc 2100 agtgatgaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2160 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2220 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 2262 <210> SEQ ID NO 172 <211> LENGTH: 154 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 172 Met Trp Gly Trp Met Gly Pro Pro Leu Pro Phe Pro Trp Lys Glu Ala 1 5 10 15 Arg Ser Pro Ala Thr Ser His Ser Ala Met His Ala Leu Ala Gly Leu 20 25 30 Ala Ser Trp Glu Thr Gln Val Thr Arg Met Asn Ser Ala Phe Ser Thr 35 40 45 Cys Leu Leu Leu Leu Gln Asp Leu Gly Val Pro Leu Thr Leu Thr Gly 50 55 60 Leu Pro Pro Ala Leu Gly Leu Ala Pro Pro Val Leu Glu Pro Arg Ala 65 70 75 80 Pro Gly Leu Glu Leu Pro Leu Trp Gly Gly Ser Gln Ala Pro Pro Leu 85 90 95 Pro Leu Leu Ser Ser Val Pro Cys Ser Ala Pro Pro Met Tyr Leu Ser 100 105 110 Val Phe Arg Pro Leu Thr Glu Arg Arg Cys Arg Val Ser Arg Gly Pro 115 120 125 Arg Trp Ser Gln Gly Gln Gly Trp Asp Leu Gln Gly Thr Arg Gly Ala 130 135 140 His Gly Leu Arg His Leu Cys Pro Gly Ser 145 150 <210> SEQ ID NO 173 <211> LENGTH: 2538 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 173 gaaaagtgga gatagttcct gtctcatgga ttgctagggg gattaagagg agtgcctgta 60 gaacacatag ctcaggtgct agtgcacagc aggtgtgtcc cagaggtgag ctgtggttgt 120 tagtctttgt gagtggagag ctgggctagg tcccaggcct gactctgtct gatgttgttt 180 ctcctctgca ctgtagtact ttattcccag attctgcttt ttaattcttt tttggtgtaa 240 ttacaagaat aaggactttg gggtcaaact gaggcttgag ctgcagagat ggaggatgca 300 ggtctggctg gtgggcatag tggtttcccc tagggctggg ggaggttggg gagggaggag 360 ggtgtgggct gcctcggtgc atctctctga caggtcctgg ccctgggtca gtccaagatg 420 cttgttcagc ctgtggagtc cagtaggatg agggttgtct gtcgagtggg tctggaggca 480 cacccccacc tcttccctag ttattgggct gggagttgct gtcagactcc aatatccaga 540 ggaattacct tgattcttcc tcttaaaacc taagatgcca ggactaccct gttccccacg 600 tccccatgcc tgcctggccc tgcagtaatg tagtggcttc catctgttga gtcctgctgt 660 gagtagacgt cccatgaggc catttaattc tttctacatt cactccttgc gcagtgggtg 720 ttagcatcct tattttgcag atgagaaagc tgaggcctgg agaagctaaa tgatgtgccc 780 ggagttctag agctggtagg tgttagctgc cgacctaccc gccccttcta cacaccttgc 840 cacctgttgg accttccatc aaggccttgg gtccaatgtt acccactcat cacagtcaaa 900 aaacttcctc ctccagccag aattaacccg tccttccttc attgtctgac tgctgtttgt 960 catttatctc tcatgaaaga gtcaggtgtt ccagatgctt gcgttcattt ttcccttccc 1020 catgaaactg tgggcttctt ggaagcagga tatgtcatga acgcatctct gacttgctga 1080 tagaggatag agcaaaggat agaaagaaca cagcaccctg gcaggatgaa tctgcccctc 1140 tccagtcaag gtggggcttc ttgggaaagt tcttgaagca gattttcagt acagcaactc 1200 agagtggctc tcaatttttg agactcagtt ccccctttta aaatggggga atgacccctg 1260 tctggccaat tgttaggggc agatgggatg aagtatgtag aattagcctg aaaactggaa 1320 tggctgtacc tgtgtttggc tggtggttgg ttggtttatc catatttatc ggatgcccgc 1380 tgtgctccca gtgttgggtt ctgccctggg acaccatgga gaaccaacag atggagccct 1440 tgcctcctcg gagctcgcag cctggagggt cggtgtttgc aggttccccc ttcaggctgg 1500 ccgggtttcc aggcctctgt gcggcatcag caccttatca tttgctgtct gtcctaggca 1560 gactccagtt ctccagccag tctcagcctc atgacctcag acaatctcac ccagccttgg 1620 tctgctgagt cacagaatgg aaactggtgc tcactcccct ggccagggta gcatgagaat 1680 cagtgaggta gggtggaaaa gggctctcta ggtggctaac aattgggaac tctaggacag 1740 gtcagaactt gagtttgcag accagccctc tacaggacac tggtggacac agagtgttaa 1800 atcctgggct tgaggactgc tttgggcagc ccttttcttg tacctgttgc cgattctggt 1860 ggcttaagct ttcttcttgg agtgaatacc tactcattgt ctcaggcaat acaggccaac 1920 aactttcctc tttcagcaag tctgcagggt gtctcctgtc ccagcttcat acctctccct 1980 ccccactctt cccattccca ctctctccat ggctctggct gctatgcact cagaatacgg 2040 aagagctatt tgctggggtg gggtagagaa aactaaattc ccattgcttg atgttggctg 2100 agcaggtggc actgttggag actcgcctcc tattcctctt tctcctcctc attttttttc 2160 attatcctac agtgatcaat tgagcattgt taggtactgg accaatcatc tttttaaaaa 2220 tgaatcatct taacagccat gcacctgtag tcccagctag tggtgaggct gagacaggag 2280 gattgcttga agccaggagg attgcttgaa gccaggagtt caagaccagc ctgggtaaca 2340 tagtgatact ctgtctttac ttttaaaatt taaaaattag ctaggttgat ggtgtgcacc 2400 tgtagtctca gctactaggg aggctgaggg ggaggatcgc ttgggcccgg gagttcaagg 2460 atgcagtgaa ctgtagtcaa gccactgtac tccagcctgg gtgacagagc aagattccgt 2520 ctcaaaaaaa aaaaaaaa 2538 <210> SEQ ID NO 174 <211> LENGTH: 125 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 174 Met Thr Pro Val Trp Pro Ile Val Arg Gly Arg Trp Asp Glu Val Cys 1 5 10 15 Arg Ile Ser Leu Lys Thr Gly Met Ala Val Pro Val Phe Gly Trp Trp 20 25 30 Leu Val Gly Leu Ser Ile Phe Ile Gly Cys Pro Leu Cys Ser Gln Cys 35 40 45 Trp Val Leu Pro Trp Asp Thr Met Glu Asn Gln Gln Met Glu Pro Leu 50 55 60 Pro Pro Arg Ser Ser Gln Pro Gly Gly Ser Val Phe Ala Gly Ser Pro 65 70 75 80 Phe Arg Leu Ala Gly Phe Pro Gly Leu Cys Ala Ala Ser Ala Pro Tyr 85 90 95 His Leu Leu Ser Val Leu Gly Arg Leu Gln Phe Ser Ser Gln Ser Gln 100 105 110 Pro His Asp Leu Arg Gln Ser His Pro Ala Leu Val Cys 115 120 125 <210> SEQ ID NO 175 <211> LENGTH: 2371 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (285) <400> SEQUENCE: 175 tgacttccag gtgaagggat gggaaaagtg gactctcatt gtagtgactc ccaacctacc 60 taataatttg ttaacttagg aatatgctat cattgttgac ttgttcttcc ttaggagaag 120 gacgattttc acccaccctt tctgttctat ggtggactct taacaggtgc tatgtgacca 180 ggaatctagc cgggagtagc agaggccctg tcttctgaag tctcaggctt agaagttacc 240 aaagtgggct cagaaactgt catctcctgg ttccaagttc gggcnctggc agcccagccg 300 ctatcttagc tgtctttccc agcggtgcta agagtggtct cagtgagaag gtagatgcca 360 actggagggc cagacctgtg tcctgtccca tgtcctcctt ggtggacgtt tctgtttact 420 cagagctgct agagaccatc ctgcccatcc gagttctgag attgggactg tgatgttggg 480 acctgaggac tggatggtag aatactgggg tcccccagct cttagcagga tgcaggctat 540 tgcttccaca cccctggccg tgagaacgtg gtatgtagga gagttggctg tagctttagg 600 atttctggaa gccaatttgg catggcctat ttgatctctg gcttgtgctc ctgctacact 660 gacagactga ttgcgtggct ctttcagaag acccaggaag ggcagctcca gccagaggac 720 cttcctggct atgcaggtgc acagctctta ggcatcaagc aaagggtcag ccagtcagta 780 gtagtgggag gaagcccttc ctcctcttat gcaagcagct cgcagccagc ccagaatctc 840 ttatgcagcc caaagggctt cttgaggtag agagccctcc ccagtgtctt cccaggataa 900 gtagaaatat gatcacagag caacggagca aaagctttcg ggagtgtgag gctgcatctg 960 ctggagcaaa aggaaaccgt gggcttttcc ggccagatac tcttgagctc tgtgaccctg 1020 ctcctgtcac cccaatttct ccaagccaga ggtagctttc tcagagcccc ttggtggttc 1080 tgtcctccaa atgctgctgt tgggagcggg cttccagctc tcagtggcag tgcacctcct 1140 cctaaatgca ggcacttgct aggaagagtg tgagctggcg tcttctgttc accctgccta 1200 gcagttgtca ccattcacaa gtggcattat ttatgttgtg ctgctgtcca gctgctaaga 1260 tcccttcatc tgcacaagcc ctggctagat atgtgtgaat gtgtggcatc atttcacttc 1320 agccgcccaa ttccatctct cctctgcagc cagattcact ggctgatgct cactgctcac 1380 tgtctatccc cacgaaattt agttttatca gtagtcttaa agtgttgatc tcaaacaagt 1440 acattagaaa aatcatgttt cttctctctc atcttacttt ttcttctcag atttctccct 1500 tcctagaaca ttctctctgt ttagcactaa tgttcacctc gtattttttg gaagtgcaaa 1560 aatctcaatt tgtgtctgtt tacagctctc tctcctcact gctcacagca aggggttctg 1620 tatcagtgga tttcattttg tagctgttga gatgttaagg caagcctcag catctgcccc 1680 tgctgggtgc acaatgctgc ttcctcgaag agaagacaca gagtccaagt ggcaggactt 1740 gaggttggct tcccactctg ccttagaagt taattttcca aagtacatta caaatctctg 1800 aggccattag gggaaaagga aggggtgtgg tttgtctttg aaattacagt taatactttt 1860 agacagtaag tccggctggt tgcagggcta tttgccccga cagcatcagc ctgtaacatt 1920 tcttctcttt cctttgtgcc actgagtcgt tccctggcca gaggacataa atggtgctgg 1980 taggaggtta tcagagtaag gaaggtagca gatataggtg cagggtgcct gtcattcact 2040 gtgttatttg gtttaaatca aagtgattct gggggaagct atgctctttc agtggataat 2100 aaaattggta actctattgt aaaacatgtc aatggtgtgt gaagaaaaat caaccaatct 2160 gtaggtgttg ataactagac agtactgtgt atgttacgtg cctgtgtgga tgtgcacttc 2220 cagcatggta tgtgtagcga tgtggatcat gccagagttc gtagatcctg ttttggggtt 2280 tgcacatgga tcgtatgtta agctttttct tttcaataaa tgaattttat ttttattttc 2340 gaaaaaaaaa aaaaaaaaaa aaaaaaaaaa a 2371 <210> SEQ ID NO 176 <211> LENGTH: 114 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 176 Met Cys Gly Ile Ile Ser Leu Gln Pro Pro Asn Ser Ile Ser Pro Leu 1 5 10 15 Gln Pro Asp Ser Leu Ala Asp Ala His Cys Ser Leu Ser Ile Pro Thr 20 25 30 Lys Phe Ser Phe Ile Ser Ser Leu Lys Val Leu Ile Ser Asn Lys Tyr 35 40 45 Ile Arg Lys Ile Met Phe Leu Leu Ser His Leu Thr Phe Ser Ser Gln 50 55 60 Ile Ser Pro Phe Leu Glu His Ser Leu Cys Leu Ala Leu Met Phe Thr 65 70 75 80 Ser Tyr Phe Leu Glu Val Gln Lys Ser Gln Phe Val Ser Val Tyr Ser 85 90 95 Ser Leu Ser Ser Leu Leu Thr Ala Arg Gly Ser Val Ser Val Asp Phe 100 105 110 Ile Leu <210> SEQ ID NO 177 <211> LENGTH: 1665 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1633) <400> SEQUENCE: 177 atggcagcgc ccagcaacaa gacagagctg gcctggagtc cgcggctggc cgcgtgagta 60 ggtgattgtc tgacaagcag aggcatgagc tgggtccagg ccaccctact ggcccgaggc 120 ctctgtaggg cctggggagg cacctgcggg gccgccctca caggaacctc catctctcag 180 gtccctcgcc ggctccctcg gggcctccac tgcagcgcag ctgcccatag ctctgaacag 240 tccctggttc ccagcccacc ggaaccccgg cagaggccca ccaaggctct ggtgcccttt 300 gaggacctgt ttgggcaggc gcctggtggg gaacgggaca aggcgagctt cctgcagacg 360 gtgcagaaat ttgcggagca cagcgtgcgt aagcggggcc acattgactt catctacctg 420 gccctgcgca agatgcggga gtatggtgtc gagcgggacc tggctgtgta caaccagctg 480 ctcaacatct tccccaagga ggtcttccgg cctcgcaaca tcatccagcg catcttcgtc 540 cactaccctc ggcagcagga gtgtgggatt gctgtcctgg agcagatgga gaaccacggt 600 gtgatgccca acaaggagac ggagttcctg ctgattcaga tctttggacg caaaagctac 660 cccatgctca agttggtgcg cctgaagctg tggttccctc gattcatgaa cgtcaacccc 720 ttcccagtgc cccgggacct gccccaggac cctgtggagc tggccatgtt tggcctgcgg 780 cacatggagc ctgaccttag tgccagggtc accatctacc aggttccttt gcccaaagac 840 tcaacaggtg cagcagatcc cccccagccc cacatcgtag gaatccagag tcccgatcag 900 caggccgccc tggcccggca caatccagcc cggcctgtct ttgttgaggg ccccttctcc 960 ctgtggctcc gcaacaagtg tgtgtattac cacatcctca gagctgactt gctgcccccg 1020 gaggagaggg aagtggaaga gacgccggag gagtggaacc tctactaccc gatgcagctg 1080 gacctggagt atgtgaggag tggctgggac aactacgagt ttgacatcaa tgaagtggag 1140 gaaggccctg tcttcgccat gtgcatggcg ggtgctcatg accaggcgac gatggctaag 1200 tggatccagg gcctgcagga gaccaaccca accctggccc agatccccgt ggtcttccgc 1260 ctcgccgggt ccacccggga gctccagaca tcctctgcag ggctggagga gccgcccctg 1320 cccgaggacc accaggaaga agacgacaac ctgcagcgac agcagcaggg ccagagctag 1380 tctgagccgg cgcgagggca cgggctgtgg cccgaggagg cggtggactg aaggcatgag 1440 atgccctttg agtgtacagc aaatcaatgt tttcctgctt ggggctctct tccctcatct 1500 ctagcagtat ggcatcccct ccccaggatc tcgggctgcc agcgatgggc aggcgagacc 1560 cctccagaat ctgcaggcgc ctctggttct ccgaattcaa ataaataggt gcgggagcgc 1620 tgttggttgt gcncgaaaaa aaaaaaaaaa aaaaaaaaaa aaaaa 1665 <210> SEQ ID NO 178 <211> LENGTH: 431 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 178 Met Ser Trp Val Gln Ala Thr Leu Leu Ala Arg Gly Leu Cys Arg Ala 1 5 10 15 Trp Gly Gly Thr Cys Gly Ala Ala Leu Thr Gly Thr Ser Ile Ser Gln 20 25 30 Val Pro Arg Arg Leu Pro Arg Gly Leu His Cys Ser Ala Ala Ala His 35 40 45 Ser Ser Glu Gln Ser Leu Val Pro Ser Pro Pro Glu Pro Arg Gln Arg 50 55 60 Pro Thr Lys Ala Leu Val Pro Phe Glu Asp Leu Phe Gly Gln Ala Pro 65 70 75 80 Gly Gly Glu Arg Asp Lys Ala Ser Phe Leu Gln Thr Val Gln Lys Phe 85 90 95 Ala Glu His Ser Val Arg Lys Arg Gly His Ile Asp Phe Ile Tyr Leu 100 105 110 Ala Leu Arg Lys Met Arg Glu Tyr Gly Val Glu Arg Asp Leu Ala Val 115 120 125 Tyr Asn Gln Leu Leu Asn Ile Phe Pro Lys Glu Val Phe Arg Pro Arg 130 135 140 Asn Ile Ile Gln Arg Ile Phe Val His Tyr Pro Arg Gln Gln Glu Cys 145 150 155 160 Gly Ile Ala Val Leu Glu Gln Met Glu Asn His Gly Val Met Pro Asn 165 170 175 Lys Glu Thr Glu Phe Leu Leu Ile Gln Ile Phe Gly Arg Lys Ser Tyr 180 185 190 Pro Met Leu Lys Leu Val Arg Leu Lys Leu Trp Phe Pro Arg Phe Met 195 200 205 Asn Val Asn Pro Phe Pro Val Pro Arg Asp Leu Pro Gln Asp Pro Val 210 215 220 Glu Leu Ala Met Phe Gly Leu Arg His Met Glu Pro Asp Leu Ser Ala 225 230 235 240 Arg Val Thr Ile Tyr Gln Val Pro Leu Pro Lys Asp Ser Thr Gly Ala 245 250 255 Ala Asp Pro Pro Gln Pro His Ile Val Gly Ile Gln Ser Pro Asp Gln 260 265 270 Gln Ala Ala Leu Ala Arg His Asn Pro Ala Arg Pro Val Phe Val Glu 275 280 285 Gly Pro Phe Ser Leu Trp Leu Arg Asn Lys Cys Val Tyr Tyr His Ile 290 295 300 Leu Arg Ala Asp Leu Leu Pro Pro Glu Glu Arg Glu Val Glu Glu Thr 305 310 315 320 Pro Glu Glu Trp Asn Leu Tyr Tyr Pro Met Gln Leu Asp Leu Glu Tyr 325 330 335 Val Arg Ser Gly Trp Asp Asn Tyr Glu Phe Asp Ile Asn Glu Val Glu 340 345 350 Glu Gly Pro Val Phe Ala Met Cys Met Ala Gly Ala His Asp Gln Ala 355 360 365 Thr Met Ala Lys Trp Ile Gln Gly Leu Gln Glu Thr Asn Pro Thr Leu 370 375 380 Ala Gln Ile Pro Val Val Phe Arg Leu Ala Gly Ser Thr Arg Glu Leu 385 390 395 400 Gln Thr Ser Ser Ala Gly Leu Glu Glu Pro Pro Leu Pro Glu Asp His 405 410 415 Gln Glu Glu Asp Asp Asn Leu Gln Arg Gln Gln Gln Gly Gln Ser 420 425 430 <210> SEQ ID NO 179 <211> LENGTH: 2080 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 179 ctccggccgg cgtccagttt gagtctaggt tggagttgga accgtggaga tgcggaagga 60 aaccccaccc cccctagtgc ccccggcggc ccgggagtgg aatcttcccc caaatgcgcc 120 cgcctgcatg gaacggcagt tggaggctgc gcggtaccgg tccgatgggg cgcttctcct 180 cggggcctcc agcctgagtg ggcgctgctg ggccggctcc ctctggcttt ttaaggaccc 240 ctgtgccgcc cccaacgaag gcttctgctc cgccggagtc caaacggagg ctggagtggc 300 tgacctcact tgggttgggg agagaggtat tctagtggcc tccgattcag gtgctgttga 360 attgtgggaa ctagatgaga atgagacact tattgtcagc aagttctgca agtatgagca 420 tgatgacatt gtgtctacag tcagtgtctt gagctctggc acacaagctg tcagtggtag 480 caaagacatc tgcatcaagg tttgggacct tgctcagcag gtggtactga gttcataccg 540 agctcatgct gctcaggtca cttgtgttgc tgcctctcct cacaaggact ctgtgtttct 600 ttcatgcagc gaggacaata gaattttact ctgggatacc cgctgtccca agccagcatc 660 acagattggc tgcagtgcgc ctggctacct tcctacctcg ctggcttggc atcctcagca 720 aagtgaagtc tttgtctttg gtgatgagaa tgggacagtc tcccttgtgg acaccaagag 780 tacaagctgt gtcctgagct cagctgtaca ctcccagtgt gtcactgggc tggtgttctc 840 cccacacagt gttcccttcc tggcctctct cagtgaagac tgctcacttg ctgtgctgga 900 ctcaagcctt tctgagttgt ttagaagcca agcccacaga gactttgtga gagatgcgac 960 ttggtccccg ctcaatcact ccctgcttac cacagtgggc tgggaccatc aggtcgtcca 1020 ccacgttgtg cccacagaac ctctcccagc ccctggacct gcaagtgtta ctgagtagat 1080 tggatttaag acaaaaagca agtcccccat gagtgtccac ttctttgccc tgccctctca 1140 gcttgtgaga caacacagga gccttctata gtatgttgat atgctagatc tgtgccgtta 1200 ataggcatcg tctctcagcc tgagggaggc tggattctgg gttcctgtag tcacagggag 1260 gaaaagcttt cttaaaaatg gacatgtatg tgcgtgtgag tgtgtgtgta gatttatagt 1320 ttttggtagt ggcaggaata aaaaaaatcc atcctacatc ttccctaagc actgcctctc 1380 tctcaccccc caaaacaagt tgacgaaagg gttttatgta gctgtctatg aggaattggc 1440 cgtgtctggg tgggttatgg gatgtgggca tccctgggtt cttggaagca gctcttatgc 1500 tactcataga gatgggattg actttatttt tttatagtgc ttaattcacc attatgagaa 1560 atgcttccag tcacaaaaat gcagcccagc tcactctgag gaagaagcag gacttggtac 1620 ggttttacac aactccttac cattaaactg aatcagaaat ccattttctg gctgaataaa 1680 aagtttggct tgcctgtgta atgcccactc ccttccccct ggctccctag tgatgggaca 1740 tatatgagac agaagtgttt ttctatcata gacaccatag gggaaagttt ggggatgaag 1800 gagagcttaa aggtgtttca attaagttag aaaactgaca caggctgttg agaattcttt 1860 gccacttttc ccaccccaaa acagcatggg gcctgacatc ttctgccctg gtcccctttc 1920 tcttgatgtg gaaagtctga atgcagtatt tatagacttc taaggtttta aaatccagta 1980 ttcaagaaga aaatcagaaa tactggttgg tgaaataaag agtttaggca ttgttggcct 2040 gtcttttttg aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2080 <210> SEQ ID NO 180 <211> LENGTH: 342 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 180 Met Arg Lys Glu Thr Pro Pro Pro Leu Val Pro Pro Ala Ala Arg Glu 1 5 10 15 Trp Asn Leu Pro Pro Asn Ala Pro Ala Cys Met Glu Arg Gln Leu Glu 20 25 30 Ala Ala Arg Tyr Arg Ser Asp Gly Ala Leu Leu Leu Gly Ala Ser Ser 35 40 45 Leu Ser Gly Arg Cys Trp Ala Gly Ser Leu Trp Leu Phe Lys Asp Pro 50 55 60 Cys Ala Ala Pro Asn Glu Gly Phe Cys Ser Ala Gly Val Gln Thr Glu 65 70 75 80 Ala Gly Val Ala Asp Leu Thr Trp Val Gly Glu Arg Gly Ile Leu Val 85 90 95 Ala Ser Asp Ser Gly Ala Val Glu Leu Trp Glu Leu Asp Glu Asn Glu 100 105 110 Thr Leu Ile Val Ser Lys Phe Cys Lys Tyr Glu His Asp Asp Ile Val 115 120 125 Ser Thr Val Ser Val Leu Ser Ser Gly Thr Gln Ala Val Ser Gly Ser 130 135 140 Lys Asp Ile Cys Ile Lys Val Trp Asp Leu Ala Gln Gln Val Val Leu 145 150 155 160 Ser Ser Tyr Arg Ala His Ala Ala Gln Val Thr Cys Val Ala Ala Ser 165 170 175 Pro His Lys Asp Ser Val Phe Leu Ser Cys Ser Glu Asp Asn Arg Ile 180 185 190 Leu Leu Trp Asp Thr Arg Cys Pro Lys Pro Ala Ser Gln Ile Gly Cys 195 200 205 Ser Ala Pro Gly Tyr Leu Pro Thr Ser Leu Ala Trp His Pro Gln Gln 210 215 220 Ser Glu Val Phe Val Phe Gly Asp Glu Asn Gly Thr Val Ser Leu Val 225 230 235 240 Asp Thr Lys Ser Thr Ser Cys Val Leu Ser Ser Ala Val His Ser Gln 245 250 255 Cys Val Thr Gly Leu Val Phe Ser Pro His Ser Val Pro Phe Leu Ala 260 265 270 Ser Leu Ser Glu Asp Cys Ser Leu Ala Val Leu Asp Ser Ser Leu Ser 275 280 285 Glu Leu Phe Arg Ser Gln Ala His Arg Asp Phe Val Arg Asp Ala Thr 290 295 300 Trp Ser Pro Leu Asn His Ser Leu Leu Thr Thr Val Gly Trp Asp His 305 310 315 320 Gln Val Val His His Val Val Pro Thr Glu Pro Leu Pro Ala Pro Gly 325 330 335 Pro Ala Ser Val Thr Glu 340 <210> SEQ ID NO 181 <211> LENGTH: 1313 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (1165) <400> SEQUENCE: 181 tgcttaagca cgaagcttct tttcctgttt agtcctagtg gttagtgtcg aaagaggaat 60 catcgaggtt tcttgatgaa acctagtgcg gtccaacctc tgcctttttt tctgttgtct 120 tttttcctac tccgggctgt tggcggtgtc agcaccgctg ctgggggcgg gggtggaggg 180 gagaaagagt cgggttaccg aagtgcgtca ttcctggctc tagcagggcc tgctcgggag 240 ctgctggtgt ttgttactgt cctcgcagca cttttctgcc aaccttctct ctctgcgtat 300 tggttaggag caaaagcagg aggcggtctc ctaattctgt ctgtagccta gcgcgttgcg 360 tttaagggta tatctgaact tattttgtta aaaaaaaggc tctgggaagt ggatgcattt 420 gtttaatgac atataattca ggtagtttag gcttgctctc atatactttc cgatgaacag 480 tggggttaat tttcaacatt ttcaaccact taacgttaaa atgcctggtt ttctttctac 540 attgatatca atctataatt agggatcaga aggaccagtt taaggtatat aagtgttcag 600 cagtttttca agtggttgaa ttgcagtttt atgacacatt atgttaaata gtcgattttt 660 tttttttcat tttgaactaa ggtgccacgt taagtaagtt aattgcagat gtttaagttc 720 gttttcatca catttcccta tttgtctttt taggtataat tttaaatatg ccctttgggt 780 ttatggactt cattaaaatt cttaaagatg gttatatctt tgtgtttaac tgaattctta 840 aatttatcac ctaccaaaga attgtgtaag gcgtaaggcg gctgtatagt tacattgttg 900 gattttgact taacatgcta gtttttgata cttttgctat ctttgggtag aagtgtactt 960 agagaacata gtatcttcct cttaattctt tttgaagata ataatgagag gagggagtgg 1020 gtaggaggta ggtgtgaagc agaagtggcc ttgagttgat tattgtagct ggatgaatac 1080 agaagcgctc attgttacta ttattctctc tacttttgtg cgtgctgtta aacatttcca 1140 tagtttaaga taaacttttt ttgcnagtag aatttccaga ttgtcttaca gtcttggggg 1200 taatgactta agtttatatt tacatgtcaa aattacttgc ataggaaatt tagccttgtg 1260 taagtgatta cacaatgctt ggcaaaaaaa aaaaaaaaaa aaaaaaaaaa aaa 1313 <210> SEQ ID NO 182 <211> LENGTH: 91 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 182 Met Lys Pro Ser Ala Val Gln Pro Leu Pro Phe Phe Leu Leu Ser Phe 1 5 10 15 Phe Leu Leu Arg Ala Val Gly Gly Val Ser Thr Ala Ala Gly Gly Gly 20 25 30 Gly Gly Gly Glu Lys Glu Ser Gly Tyr Arg Ser Ala Ser Phe Leu Ala 35 40 45 Leu Ala Gly Pro Ala Arg Glu Leu Leu Val Phe Val Thr Val Leu Ala 50 55 60 Ala Leu Phe Cys Gln Pro Ser Leu Ser Ala Tyr Trp Leu Gly Ala Lys 65 70 75 80 Ala Gly Gly Gly Leu Leu Ile Leu Ser Val Ala 85 90 <210> SEQ ID NO 183 <211> LENGTH: 1484 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 183 gttttcatct ctaaaagttg gatttgggtg tgtgtttcat gtcttccatt tatatatgtt 60 tttaatgaac atgcgtaata taataactac attcatgtct ttgctaattc taacatatgt 120 gccaattctg gttggttgat taataaatct cttcattatg ggtatttcct aatatattac 180 ctgtgttata attttacatt ttatgtcaga cattgtgaat ttttaccttg ttgggtgctg 240 tatatttttg tattcctgta agtgttacac tttgttctgt cacacaatta agctagtcgg 300 aaacaatttt atctttttaa gatatggtag atgggtttgg agcagtgctc agcctagaac 360 tgatttactt ttgacttcta aggcaaggcc cttttatgca gtgtatccac tgctctatgt 420 atcatgcagc tttttcagtc tggctgaggg aacaggcgtg ggtgctggcc cttttgtgca 480 tcaggccttt gttatcacag aactttcatt tggttctttt cctggcttcc tgtcatttct 540 tcacacgtgt gggttgatca gtattcacca gaatacctga ggagaccagc ccaggcaaca 600 tagtgagacc ccctttctcc ccattaaaac agacacaccc acacacccac ccacccacac 660 cccttgccca aagtcatagt ttttaggtgg tatagatgtg atttgaactt agatcccggc 720 tttgataaac cagtgttttt taaagcactt tatgttgcct gccctgtaca gcgtctttcc 780 tcttcctttt gatgagataa aatactgaaa gcataactct gaattacagt ataaaaatac 840 acattttggc ttattagggc agtgggatgt ctctgccctc ttcccccaca tttcttttat 900 gttcatgcag aaaataaaat ggaaatcctt tttctttttg caagaacatg aattataagc 960 ttataggaat catttatcat ccatgtttaa aaaattccca tctctcagct aaaagactac 1020 atcatatgac ttaattctaa taggtcaact ctactgaagt taagagcatt cccaaagaat 1080 gctctatata aaacttgtgt gtatgtttgc aggaatctta atggatatgt ttctagagga 1140 aatgctccca tgagcattct ctccatcatt tagcagctgt taaaatgatg ctcttcccaa 1200 tgcccttgtt ccctcattgt aaacgtgctc tgagttaacc tggtagccag tacacagtac 1260 acagtaaatg acatttctta tctgtatgtt agaactacta ttcaataagc taaaatattc 1320 tgagcttcct cagattttct cctttttttt tttttgggac ggagtcttgc cctgttgccc 1380 aggctggagt gcagtgagct gagatcacgc cactacactc catcctgggt ggtggagtga 1440 gaccctgtct aagcaaaaaa aaaaaaaaaa aaaaaaaaaa aaaa 1484 <210> SEQ ID NO 184 <211> LENGTH: 125 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 184 Met Ser Asp Ile Val Asn Phe Tyr Leu Val Gly Cys Cys Ile Phe Leu 1 5 10 15 Tyr Ser Cys Lys Cys Tyr Thr Leu Phe Cys His Thr Ile Lys Leu Val 20 25 30 Gly Asn Asn Phe Ile Phe Leu Arg Tyr Gly Arg Trp Val Trp Ser Ser 35 40 45 Ala Gln Pro Arg Thr Asp Leu Leu Leu Thr Ser Lys Ala Arg Pro Phe 50 55 60 Tyr Ala Val Tyr Pro Leu Leu Tyr Val Ser Cys Ser Phe Phe Ser Leu 65 70 75 80 Ala Glu Gly Thr Gly Val Gly Ala Gly Pro Phe Val His Gln Ala Phe 85 90 95 Val Ile Thr Glu Leu Ser Phe Gly Ser Phe Pro Gly Phe Leu Ser Phe 100 105 110 Leu His Thr Cys Gly Leu Ile Ser Ile His Gln Asn Thr 115 120 125 <210> SEQ ID NO 185 <211> LENGTH: 2520 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 185 cccgagtgca tctggaatac gcagagtcag taagaccatg gctacgtcct cgatgtctaa 60 gggttgcttt gtttttaagc caaactccaa aaagagaaag atctctctgc caatagagga 120 ctattttaac aaagggaaaa atgagcctga ggacagtaag cttcgattcg aaacttatca 180 gttgatatgg cagcagatga aatctgaaaa tgagcgacta caagaggaat taaataaaaa 240 cttgtttgac aatctgattg aatttctgca aaaatcacat tctggattcc agaagaattc 300 aagagacttg ggcggtcaaa taaaactcag agaaattcca actgctgctc ttgttcttgg 360 tgtgaatgtc acagatcatg atttgacatt cggaagtcta acagaggccc ttcagaataa 420 tgtcacacca tatgtagtct cattgcaagc taaagattgt ccagatatga aacatttttt 480 gcaaaagttg atctcacagt tgatggactg ctgtgtagat ataaaatcca aagaggagga 540 aagtgttcac gtcacccaaa gaaagacaca ttattcaatg gattcacttt ccagttggta 600 tatgactgtc acacagaaga cggacccaaa aatgctaagc aaaaaaagga ctacttctag 660 ccaatggcag tctcctcctg ttgtcgttat cttgaaggat atggaaagct ttgccacaaa 720 agtactacaa gacttcataa ttatcagcag tcaacatctc catgaatttc cactaatact 780 catttttgga atagccacat ctcctattat catccaccga ttgcttcctc atgcagtatc 840 atctctattg tgcatagaac tgttccaatc tttgtcttgt aaggagcacc tgactacggt 900 actcgataag ctacttctta caactcagtt tccctttaaa ataaatgaaa aagtattaca 960 ggttctgacc aacatctttt tgtatcatga tttctcagtt caaaacttta taaaaggact 1020 tcagctttct ctattagagc atttctattc ccagccctta agtgtcctgt gctgtaatct 1080 tccagaagcc aaaagaagaa taaatttttt atcaaataat caatgtgaaa acatccgacg 1140 tctaccatct tttaggaggt acgtggaaaa gcaagcttca gaaaagcaag ttgcgctctt 1200 gaccaatgag agatatttga aggaggaaac acaattatta ctagaaaacc tgcatgttta 1260 tcatatgaat tacttcctgg ttttgagatg tcttcataag ttcacctctt ctcttcccaa 1320 gtatccacta ggtcgacaga tcagagagtt gtactgtaca tgtttagaaa agaacatatg 1380 ggattcagag gagtatgcat cagtcttgca gctgctgagg atgttggcaa aggatgaact 1440 gatgaccata cttgagaaat gtttcaaggt ttttaagtct tattgtgaaa accaccttgg 1500 cagcacagct aagagaatag aggagttcct ggcccagttt cagagcctcg atgaaaccaa 1560 agaggaagaa gatgcttctg ggtcacagcc aaaggggctt cagaagacag acctctatca 1620 tcttcagaag tccttattgg aaatgaagga gttaagaaga agtaagaagc aaaccaaatt 1680 tgaagtactc agagaaaatg ttgtgaactt cattgactgt ctagtgagag aataccttct 1740 gcctcctgag acacagcctc tccatgaggt ggtgtacttc agtgctgccc atgcccttcg 1800 tgagcattta aatgctgctc cgcgaattgc cctccatact gcactcaaca atccttacta 1860 ttatctcaag aatgaagcac tgaaaagcga agaaggctgc attccgaata tcgccccaga 1920 catctgcata gcatacaaac tgcacctaga gtgtagcagg ctcatcaacc tcgtggactg 1980 gtcagaggct tttgcaacag ttgtgacagc tgctgaaaaa atggatgcaa attctgcaac 2040 ctcagaagaa atgaatgaaa ttatccatgc tcggtttatt agagctgttt ctgaactaga 2100 acttttagga tttataaaac ctaccaaaca gaagactgac catgtggcaa gactaacatg 2160 gggaggctgc tagaaagcaa ataagcaaag ccagaactat cacatttagc ttaagagaaa 2220 aaggtgacca gtcatattta catatattag aggagcctgt tttgttgaga agataaatgt 2280 gtaaccccca ttgatgttta accagaaaag tacattgcta accccaaaca ggcatgtatc 2340 aaaacacctg tggagtactt tagactccaa caaataataa tgtaactaaa actgctcaca 2400 cattttactg tactttccaa agtcattact aaattgtgag taaatcattc ttgaacttag 2460 agtatgtaaa tgtaataaat tccgttatcc aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2520 <210> SEQ ID NO 186 <211> LENGTH: 711 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 186 Met Ala Thr Ser Ser Met Ser Lys Gly Cys Phe Val Phe Lys Pro Asn 1 5 10 15 Ser Lys Lys Arg Lys Ile Ser Leu Pro Ile Glu Asp Tyr Phe Asn Lys 20 25 30 Gly Lys Asn Glu Pro Glu Asp Ser Lys Leu Arg Phe Glu Thr Tyr Gln 35 40 45 Leu Ile Trp Gln Gln Met Lys Ser Glu Asn Glu Arg Leu Gln Glu Glu 50 55 60 Leu Asn Lys Asn Leu Phe Asp Asn Leu Ile Glu Phe Leu Gln Lys Ser 65 70 75 80 His Ser Gly Phe Gln Lys Asn Ser Arg Asp Leu Gly Gly Gln Ile Lys 85 90 95 Leu Arg Glu Ile Pro Thr Ala Ala Leu Val Leu Gly Val Asn Val Thr 100 105 110 Asp His Asp Leu Thr Phe Gly Ser Leu Thr Glu Ala Leu Gln Asn Asn 115 120 125 Val Thr Pro Tyr Val Val Ser Leu Gln Ala Lys Asp Cys Pro Asp Met 130 135 140 Lys His Phe Leu Gln Lys Leu Ile Ser Gln Leu Met Asp Cys Cys Val 145 150 155 160 Asp Ile Lys Ser Lys Glu Glu Glu Ser Val His Val Thr Gln Arg Lys 165 170 175 Thr His Tyr Ser Met Asp Ser Leu Ser Ser Trp Tyr Met Thr Val Thr 180 185 190 Gln Lys Thr Asp Pro Lys Met Leu Ser Lys Lys Arg Thr Thr Ser Ser 195 200 205 Gln Trp Gln Ser Pro Pro Val Val Val Ile Leu Lys Asp Met Glu Ser 210 215 220 Phe Ala Thr Lys Val Leu Gln Asp Phe Ile Ile Ile Ser Ser Gln His 225 230 235 240 Leu His Glu Phe Pro Leu Ile Leu Ile Phe Gly Ile Ala Thr Ser Pro 245 250 255 Ile Ile Ile His Arg Leu Leu Pro His Ala Val Ser Ser Leu Leu Cys 260 265 270 Ile Glu Leu Phe Gln Ser Leu Ser Cys Lys Glu His Leu Thr Thr Val 275 280 285 Leu Asp Lys Leu Leu Leu Thr Thr Gln Phe Pro Phe Lys Ile Asn Glu 290 295 300 Lys Val Leu Gln Val Leu Thr Asn Ile Phe Leu Tyr His Asp Phe Ser 305 310 315 320 Val Gln Asn Phe Ile Lys Gly Leu Gln Leu Ser Leu Leu Glu His Phe 325 330 335 Tyr Ser Gln Pro Leu Ser Val Leu Cys Cys Asn Leu Pro Glu Ala Lys 340 345 350 Arg Arg Ile Asn Phe Leu Ser Asn Asn Gln Cys Glu Asn Ile Arg Arg 355 360 365 Leu Pro Ser Phe Arg Arg Tyr Val Glu Lys Gln Ala Ser Glu Lys Gln 370 375 380 Val Ala Leu Leu Thr Asn Glu Arg Tyr Leu Lys Glu Glu Thr Gln Leu 385 390 395 400 Leu Leu Glu Asn Leu His Val Tyr His Met Asn Tyr Phe Leu Val Leu 405 410 415 Arg Cys Leu His Lys Phe Thr Ser Ser Leu Pro Lys Tyr Pro Leu Gly 420 425 430 Arg Gln Ile Arg Glu Leu Tyr Cys Thr Cys Leu Glu Lys Asn Ile Trp 435 440 445 Asp Ser Glu Glu Tyr Ala Ser Val Leu Gln Leu Leu Arg Met Leu Ala 450 455 460 Lys Asp Glu Leu Met Thr Ile Leu Glu Lys Cys Phe Lys Val Phe Lys 465 470 475 480 Ser Tyr Cys Glu Asn His Leu Gly Ser Thr Ala Lys Arg Ile Glu Glu 485 490 495 Phe Leu Ala Gln Phe Gln Ser Leu Asp Glu Thr Lys Glu Glu Glu Asp 500 505 510 Ala Ser Gly Ser Gln Pro Lys Gly Leu Gln Lys Thr Asp Leu Tyr His 515 520 525 Leu Gln Lys Ser Leu Leu Glu Met Lys Glu Leu Arg Arg Ser Lys Lys 530 535 540 Gln Thr Lys Phe Glu Val Leu Arg Glu Asn Val Val Asn Phe Ile Asp 545 550 555 560 Cys Leu Val Arg Glu Tyr Leu Leu Pro Pro Glu Thr Gln Pro Leu His 565 570 575 Glu Val Val Tyr Phe Ser Ala Ala His Ala Leu Arg Glu His Leu Asn 580 585 590 Ala Ala Pro Arg Ile Ala Leu His Thr Ala Leu Asn Asn Pro Tyr Tyr 595 600 605 Tyr Leu Lys Asn Glu Ala Leu Lys Ser Glu Glu Gly Cys Ile Pro Asn 610 615 620 Ile Ala Pro Asp Ile Cys Ile Ala Tyr Lys Leu His Leu Glu Cys Ser 625 630 635 640 Arg Leu Ile Asn Leu Val Asp Trp Ser Glu Ala Phe Ala Thr Val Val 645 650 655 Thr Ala Ala Glu Lys Met Asp Ala Asn Ser Ala Thr Ser Glu Glu Met 660 665 670 Asn Glu Ile Ile His Ala Arg Phe Ile Arg Ala Val Ser Glu Leu Glu 675 680 685 Leu Leu Gly Phe Ile Lys Pro Thr Lys Gln Lys Thr Asp His Val Ala 690 695 700 Arg Leu Thr Trp Gly Gly Cys 705 710 <210> SEQ ID NO 187 <211> LENGTH: 3116 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 187 gggttctctt gcaatggtta tagaaggctt gaagtacatc tggattcctt atgtgtgcat 60 gttagcagca tttggtgtat gttctcccga actttggatg acacttttca agtggcttcg 120 attaagaact gtacacccaa tattgttggc tcttattctg agcatggccg tgcctactat 180 aataggtctc agcttatgga aagagttttt tcccagatta atgacagaat taatggaact 240 acaggaattc tatgacccag atacagtgga acttatgacc tggataaaaa ggcaagctcc 300 agttgcagct gtgtttgcag ggagtccaca gttaatgggt gcgattaaat tatgcactgg 360 atggatggtg acaagtttgc ctctttacaa tgatgatgat cttctcaaga gaaatgaaaa 420 tatctaccaa atctattcaa agcgatctgc tgaggatatt tataaaatac tgacatctta 480 caaagctaat tacctaattg tagaggatgc tatctgcaat gaggtgggac ccatgagagg 540 ctgtagggtt aaagatttat tagacattgc aaatggccac atggtttgtg aagaaggtga 600 caagctaacc tactcaaaat atgggcgatt ttgtcatgag gtcaaaatta actattctcc 660 atatgtgaat tatttcacta gagtatactg gaacagatcc tactttgtat ataaaatcaa 720 cactgtgata tccttccagt cttgaaaaat aacagagcct tcatttcaaa gactacctga 780 agtaaaatgc agttttcttc tacctactcg gtgtcttttg cagatcagag tatggacatt 840 cgaaatattg ctgcttcttt cccccttctg ctgttaactg gatccagagt tctgtgggaa 900 atagaagatc aagcattact gtcctttgat taaatgtgat atctaccact ctgcaatatt 960 ccagacaggt gtcttcctta ccgttacatg gtctttaaca cttttactga ttgcaatatt 1020 ttccccataa aatcttcatt ctattataat attgatcttg aatttgaata tgtgcaaggt 1080 cagatacatt tctcaaacat aacatttaat aaataatgtg atataattat ttaatagaaa 1140 gaataattcc gaccttcaag caagtttctg aaggtatttt atgatgtata acaactgaag 1200 ttttacaata aaaactaatt taaatgttag ctgaagatat gtggcattta aattaaaatg 1260 gaaattatat aaaggaaagt gatttttaag gatatacata aagatatatt tagaattttc 1320 atgatactgt tctcctcatc tactgcttat gttaagtgag aactttctta gtaatacata 1380 atgcatgatg ttactgcatt ttctaaatga ctagtaagtg attagttttt tcacttatgc 1440 ctattaattt gataccaatt taatcatgat aaaacaataa ccgttaacat atattttgtt 1500 aaatggacat ttaaaagaat gttgttcagg tttttttttt aaatactgat atggggcata 1560 caatctattc acatgttttc tactgaagta ctaagtaaaa aaattaaatc attatcagaa 1620 taaaaatatg tgttctaaaa ttagcaacaa tttctgggga tacatgcaga tgttgttaaa 1680 cgtacctctg catacagata tattataaaa cacaagcaat gttatttatg aaactgtgat 1740 gcagtcttca acatcaagaa aaaatgacaa ctataataaa atttacaaca cagtttcaca 1800 gtctaaatgc tatgttcctt taagtatttt catattttta atcatttatt aagagaaaat 1860 tgtgaaaagt taatttggcc ttatagagag attcaggata gatgtagcct atagatgtgt 1920 cattttaata agttgggata catgtttagt ttttccttat attcctgttc agtgaacaga 1980 ttttcataat tctcacttgt taaagtgctg caaaaattgc attttcagta ctctaaatta 2040 ctacattaga agagagcatt tctccattgt ctttattttc tgttatatat gtgttgtaaa 2100 agtacactac attagaaggg agcttttccg ttgtctttat tttctgttat acatgtgttg 2160 ttaaagtaca tgcattctta gactaactct cagatgcttt gctcttttgg agctgaagaa 2220 ttgtttgatg gtgatgtcat atatctgata gattagtttc agtggttctc atttcacttt 2280 tatacgtaat ttcttaacta tattaagata gttgcaggca gtgtacctca ggttgactct 2340 gtacatctga atagtgagtc actagtattt tgcttcaagc cttctgaaaa tataaccata 2400 gttacctaag cacacagtga atagtcacat ggtagtactt gtgattagag catgtaaaac 2460 aatgtaattg aaaagtcagc ttccatattt tgtaggggaa atagaacacc ctacttttta 2520 tctagtgtga aatatttaat cgaatttttg ttgatttata ttatgttacc tgtgctgaat 2580 taggtttggt acttgtgttt tgtttgacat attagtaagt tgcttttgct tctttctgtc 2640 aacttatttt ttaaataaaa ttgatctgga aaaattgtta atgggatgtt ttaaataatg 2700 aatttttcat ccagcatcag ttgaaaagga aaagaaagct tcattatgga aatgacaata 2760 ttgaatatga cagataagtt tatttgcttc tgttttaact gcagttaata gtactagaca 2820 actttaagtg gaaagcattt agtttatttc ttcacttatt tgtagagtga acaaatgatt 2880 cacaattcta caagtaattc cacttaggta acttacagtt gttaggtttg acaataaaga 2940 tctactatga gaggagaaga atttatgggt tttgggtgga aggaatttct caaagaaata 3000 aaaaatgttc tttgcccttg atactgcaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 3060 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaa 3116 <210> SEQ ID NO 188 <211> LENGTH: 243 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 188 Met Val Ile Glu Gly Leu Lys Tyr Ile Trp Ile Pro Tyr Val Cys Met 1 5 10 15 Leu Ala Ala Phe Gly Val Cys Ser Pro Glu Leu Trp Met Thr Leu Phe 20 25 30 Lys Trp Leu Arg Leu Arg Thr Val His Pro Ile Leu Leu Ala Leu Ile 35 40 45 Leu Ser Met Ala Val Pro Thr Ile Ile Gly Leu Ser Leu Trp Lys Glu 50 55 60 Phe Phe Pro Arg Leu Met Thr Glu Leu Met Glu Leu Gln Glu Phe Tyr 65 70 75 80 Asp Pro Asp Thr Val Glu Leu Met Thr Trp Ile Lys Arg Gln Ala Pro 85 90 95 Val Ala Ala Val Phe Ala Gly Ser Pro Gln Leu Met Gly Ala Ile Lys 100 105 110 Leu Cys Thr Gly Trp Met Val Thr Ser Leu Pro Leu Tyr Asn Asp Asp 115 120 125 Asp Leu Leu Lys Arg Asn Glu Asn Ile Tyr Gln Ile Tyr Ser Lys Arg 130 135 140 Ser Ala Glu Asp Ile Tyr Lys Ile Leu Thr Ser Tyr Lys Ala Asn Tyr 145 150 155 160 Leu Ile Val Glu Asp Ala Ile Cys Asn Glu Val Gly Pro Met Arg Gly 165 170 175 Cys Arg Val Lys Asp Leu Leu Asp Ile Ala Asn Gly His Met Val Cys 180 185 190 Glu Glu Gly Asp Lys Leu Thr Tyr Ser Lys Tyr Gly Arg Phe Cys His 195 200 205 Glu Val Lys Ile Asn Tyr Ser Pro Tyr Val Asn Tyr Phe Thr Arg Val 210 215 220 Tyr Trp Asn Arg Ser Tyr Phe Val Tyr Lys Ile Asn Thr Val Ile Ser 225 230 235 240 Phe Gln Ser <210> SEQ ID NO 189 <211> LENGTH: 839 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 189 ggtatcaggg ccgggagccc tttgggagga agggaggcgt tagaggagct gccttcggag 60 gctcagggag tccctttgga gctggttgtt tccttggccc tgcagcgcac tgctcggggc 120 tcccaaggag gttgtgtgta tggttcttaa ttcatcagga caaagacccc cagcatgtgt 180 gtaccctggg acccgatttc tctgggccca catctatctc caatacctca gcctcagatc 240 agaccctttc ttttttgtct ttcttctctt aatttttaaa tgcctctttt cttgagcatt 300 ccatctctct ttttgaccct ctcaggactg ggcttagctg tccagagccc tgccggaggg 360 tgctgggggc tgtccctctg caggcactgt gttttcctca ggggctgtcc tcagaacacc 420 cctcctgctc cctggggctc ctcagggagc catttcagct ggagtctcag gtctcaaaaa 480 caacttctcc aggaggccaa aaaaagactg ggttggcttc tggtcctcat gacggctttt 540 atcctcctgg gacactttgg gtatattcat gggcattgtt tccatctgtc ttttctacct 600 gtgccacccc tgccctgatt ccacggctgc ctcaggcagg caggcaagga gctaggccgg 660 tgcccggccc tggcagcaag gggtctttgt gcagttggag atgctgccgt tgtggcagag 720 cgtcctgcag ccccgcttcc atcagcaggc tctggggtgg gggctttgca ggggatgctc 780 tctgatgttt gttccgttgt ttaaataaaa tgcacttatt tttgtttttt tttttgcta 839 <210> SEQ ID NO 190 <211> LENGTH: 112 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 190 Met Pro Leu Phe Leu Ser Ile Pro Ser Leu Phe Leu Thr Leu Ser Gly 1 5 10 15 Leu Gly Leu Ala Val Gln Ser Pro Ala Gly Gly Cys Trp Gly Leu Ser 20 25 30 Leu Cys Arg His Cys Val Phe Leu Arg Gly Cys Pro Gln Asn Thr Pro 35 40 45 Pro Ala Pro Trp Gly Ser Ser Gly Ser His Phe Ser Trp Ser Leu Arg 50 55 60 Ser Gln Lys Gln Leu Leu Gln Glu Ala Lys Lys Arg Leu Gly Trp Leu 65 70 75 80 Leu Val Leu Met Thr Ala Phe Ile Leu Leu Gly His Phe Gly Tyr Ile 85 90 95 His Gly His Cys Phe His Leu Ser Phe Leu Pro Val Pro Pro Leu Pro 100 105 110 <210> SEQ ID NO 191 <211> LENGTH: 491 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 191 gtcagggcca gggccagaga gccggagaga ggagcccccg accgagagcc caggtagagc 60 gcacagaggt gcttcgctcc tgttccagcc ctgtcttctc ccgggtgctg gcccttgagt 120 atttttttga ggagaagcag cccctgcagt tccacgtgtt cgatgccgag gacggagcca 180 ccagccctag cccgtgactg cctccctccg gaccgacact ccctcagcct ctcagtgcct 240 gtcctgaccc tcgtgactcc agtgaccaat gcctccacct cttggaccag gtgtgccccc 300 tgggttctgg acgtgagtgg tgggtcctgc tcctatctct ccaaacccca tacccttcaa 360 tgctgtggcc cctcagtgac ttccttgggt gatcctgact ttctagccat taataaagag 420 aactgctcct agcaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 480 aaaaaaaaaa a 491 <210> SEQ ID NO 192 <211> LENGTH: 89 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 192 Met Pro Arg Thr Glu Pro Pro Ala Leu Ala Arg Asp Cys Leu Pro Pro 1 5 10 15 Asp Arg His Ser Leu Ser Leu Ser Val Pro Val Leu Thr Leu Val Thr 20 25 30 Pro Val Thr Asn Ala Ser Thr Ser Trp Thr Arg Cys Ala Pro Trp Val 35 40 45 Leu Asp Val Ser Gly Gly Ser Cys Ser Tyr Leu Ser Lys Pro His Thr 50 55 60 Leu Gln Cys Cys Gly Pro Ser Val Thr Ser Leu Gly Asp Pro Asp Phe 65 70 75 80 Leu Ala Ile Asn Lys Glu Asn Cys Ser 85 <210> SEQ ID NO 193 <211> LENGTH: 2619 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 193 atcgtgagtg ctcggtaaat atctgtggct ttaatggatg aatgaatgaa tgactacatg 60 gctaaactcc attctagggc aacatctgtg gctgcagtgg atgggcccta gtgaatggat 120 atttaacgga tatcgtacta ttcctcatct ccacagggtc aggctgtgcc acatccaccc 180 agccttgcct ggggtcattt atcctacatg tactcagatc acgtgaactg gtgatgggcc 240 acccatgtgc ctgcctggag actcctattc acccttcaga tcaatatccc ccaaataaac 300 tcccagtcac tctggcatcc catgttgctt tgtgatctct gcctctctct agaccatttg 360 gctcctatgc acaggcagct atgtcttttt catatttggg tccccaaaat gcacagtgcg 420 gtgcctgcct caaaacaaat gcttttcaat ccgtcaatca atcagttgac atggatcatc 480 ttttctcagc actgatgtat ggactacaac ttggaattcc attaaagctc ctggggtcaa 540 gaaaaaaagt gattcaagtt tatttattta tttttttttg agacagagtc tcattctgtc 600 gcccaggctg gagtgcagtg gcacgatctt ggctcactgc aacctctgcc tctggggttc 660 aagtgattct cactcatgcc tcagcctccc aagtagctgg gcaagagcca gcacacccgg 720 gctaattttt gtatttttag tagggacggg ctttcgccat gttggccaga ctggtctcga 780 gctcctggct tcaagtgatc tgcccacttc agcctcccaa agtgctggga ttacaggcat 840 ttaatcactg cacccgggtg agccactgca cccggccaag ttcatattct aaaagtgaaa 900 cattaatgct gcattgtgta ttttttggtc aagtgcttca gatgtgtgga aggaatttct 960 ttgtataaat gcaattattc gtcaccatga tgataattat aacgagggtg actgcacaga 1020 actgtgcctc cccagcaagc atgggctggg cagggccggg tattcccttc gctgacttgc 1080 ttcactagtt gactaacaga ccttattccc gggcctgagc tgatgatatc ctgccaatgc 1140 cagcttccca acatggaggg gacgcaagag cgagcgccat gggatcctgg gggaaaagca 1200 gcctgtgttt gctgctgctt tgacagttga ggctctgaga gggactggca aacaatggga 1260 aatgaaacat ttgagtggtt gcaaaaaatt ccatgggaaa tcccccctgg tggtatttat 1320 gtgcgacggc tgtgacaagg agagcgcagg gctttcgatt tcaagggttc ctgagcagac 1380 cacaatggcc ttccaagatg gcaatccccg ggaacagctc tctcggccac aaaaggccag 1440 tttgtctgtc cagggaagat ctggccccat gcatcaagtt ggccatgagc tgcagtgtct 1500 tctttggggc atgacccaca tttatagggt ctgggcctct gaaccttctg ctcctaagac 1560 agatctatct cagttgtccc tctggttttc ccaggcctca aggacctggg ggctgatggg 1620 ggctgagggg tttccctcgg gctcagcctc catctgcaga actgtgggaa cctcagcctc 1680 catcagaccc ctccccattt tctggtcagc acgtggcctc ctcctgtttc ctccattccc 1740 gttggtaatg gacatttatt taacttttac tccccctcca ttctcattta gaaaagaaag 1800 tgaactgata ttaaccaatc tttgttttgc cttctttaac actaatgcat atgcaaaata 1860 gttaccacta ttgataatat cttattgctg ctgtgatata tgtgtgtata tgtacagatc 1920 tgcttgaagg taagctttat atagattttt agagatactt ggtaaatgag aaaatggaaa 1980 ctgaaagagg ttaaataaac tgcccatgtg tattggtcat gaggtttcag ttgcaaagtg 2040 acaaaatcct gacttagatg aacttaaacc ggatggaaaa tgtacattgt attatttgag 2100 aagcaaggtc tggataagct tcaggcatgg ctggatccag gccctcagtt aagtctttag 2160 gaatttccct ctctctagct ttttggcttt gcttttccct gtattggttt catgtttaga 2220 ttggctcact tcacctgttt tacatctttc cagagtcaaa tccagccttt ttcctggttg 2280 cctccataaa agtcccaggg ttaggtttag tgtgctctga tagattcagc tgcccattgc 2340 tgaagcagtg actctggcaa cagggatgga ctgatctaag tgcccaggtt ccagtcactg 2400 ctgaagccca gccagaccac ctggacacag taagagtgag tggttccccc aaagaaaact 2460 ggggtgctct taccagaaga aggaggaatc gacaaaaaga cctgatgtcc taaactcccg 2520 tgtcacactg tcactaatgg gcaggcagac ccatacagca gctcctctgc atcttcatgc 2580 tgctagagac caccaccacg aaacaaaaaa aaaaaaaaa 2619 <210> SEQ ID NO 194 <211> LENGTH: 199 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 194 Met Lys His Leu Ser Gly Cys Lys Lys Phe His Gly Lys Ser Pro Leu 1 5 10 15 Val Val Phe Met Cys Asp Gly Cys Asp Lys Glu Ser Ala Gly Leu Ser 20 25 30 Ile Ser Arg Val Pro Glu Gln Thr Thr Met Ala Phe Gln Asp Gly Asn 35 40 45 Pro Arg Glu Gln Leu Ser Arg Pro Gln Lys Ala Ser Leu Ser Val Gln 50 55 60 Gly Arg Ser Gly Pro Met His Gln Val Gly His Glu Leu Gln Cys Leu 65 70 75 80 Leu Trp Gly Met Thr His Ile Tyr Arg Val Trp Ala Ser Glu Pro Ser 85 90 95 Ala Pro Lys Thr Asp Leu Ser Gln Leu Ser Leu Trp Phe Ser Gln Ala 100 105 110 Ser Arg Thr Trp Gly Leu Met Gly Ala Glu Gly Phe Pro Ser Gly Ser 115 120 125 Ala Ser Ile Cys Arg Thr Val Gly Thr Ser Ala Ser Ile Arg Pro Leu 130 135 140 Pro Ile Phe Trp Ser Ala Arg Gly Leu Leu Leu Phe Pro Pro Phe Pro 145 150 155 160 Leu Val Met Asp Ile Tyr Leu Thr Phe Thr Pro Pro Pro Phe Ser Phe 165 170 175 Arg Lys Glu Ser Glu Leu Ile Leu Thr Asn Leu Cys Phe Ala Phe Phe 180 185 190 Asn Thr Asn Ala Tyr Ala Lys 195 <210> SEQ ID NO 195 <211> LENGTH: 2874 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 195 gaagaaagca aaagttcaga agagatgtca gtagaaaaca aaaataggac cagagatcaa 60 gaagccccag aggatgtaca agtcaggcca gaggatactc cttcagatct cagtgttagt 120 aattccagtg tcatactgga aaacacgatg gaagaccatg ctgctgaggc atccgggaag 180 cctctaggtg aaattagtgt tccactggac agctctttac tttgtacttt gtcctcagaa 240 tctcaccagg aagcagctag taatgagaat gataaaaaac ctggtaacta caaatctatg 300 ttacgaccag aggttggcac cacttcacaa gattcagctc tcttagatca ggaattgtat 360 aactccttcc atttctggag gactcctctt cctgaaatag atctagacat agagcttgaa 420 cagaactctg ggggaaaacc cagcccagag ggaccagagg aagaatctga gggccctgtg 480 cccagttctc caaacatcac catggccacc agaaaggaac tggaagaaat gatagaaaat 540 ctagagcccc acattgatga tccagatgtt aaagcacaag tggaagtgct gtccgctgca 600 ctacgtgctt ccagcctgga tgcacatgaa gagaccatca gtatagaaaa gagaagtgat 660 ttgcaagatg aactggatat aaatgagcta ccaaattgta aaataaatca agaagattct 720 gtgcctttaa tcagcgatgc tgttgagaat atggactcca ctcttcacta tattcacagc 780 gattcagact tgagcaacaa tagcagtttt agccctgatg aggaaaggag aactaaagta 840 caagatgttg tacctcaggc gttgttagat cagtatttat ctatgactga cccttctcgt 900 gcacagacgg ttgacactga aattgctaag cactgtgcat atagcctccc tggtgtggcc 960 ttgacactcg gaagacagaa ttggcactgc ctgagagaga cgtatgagac tctggcctca 1020 gacatgcagt ggaaagttcg acgaactcta gcattctcca ttcacgagct tgcagttatt 1080 cttggagatc aattgacagc tgcagatctg gttccaattt ttaatggatt tttaaaagac 1140 ctcgatgaag tcaggatagg tgttcttaaa cacttgcatg attttctgaa gcttcttcat 1200 attgacaaaa gaagagaata tctttatcaa cttcaggagt ttttggtgac agataatagt 1260 agaaattggc ggtttcgagc tgaactggct gaacagctga ttttacttct agagttatat 1320 agtcccagag atgtttatga ctatttacgt cccattgctc tgaatctgtg tgcagacaaa 1380 gtttcttctg ttcgttggat ttcctacaag ttggtcagcg agatggtgaa gaagctgcac 1440 gcggcaacac caccaacgtt cggagtggac ctcatcaatg agcttgtgga gaactttggc 1500 agatgtccca agtggtctgg tcggcaagcc tttgtctttg tctgccagac tgtcattgag 1560 gatgactgcc ttcccatgga ccagtttgct gtgcatctca tgccgcatct gctaacctta 1620 gcaaatgaca gggttcctaa cgtgcgagtg ctgcttgcaa agacattaag acaaactcta 1680 ctagaaaaag actatttctt ggcctttgcc agctgccacc aggaggctgt ggagcagacc 1740 atcatggctc ttcagatgga ccgtgacagc gatgtcaagt attttgcaag catccaccct 1800 gccagtacca aaatctccga agatgccatg agcacagcgt cctcaaccta ctagaaggct 1860 tgaatctcgg tgtctttcct gcttccatga gagccgaggt tcagtgggca ttcgccacgc 1920 atgtgacctg ggatagcttt cgggggagga gagaccttcc tctcctgcgg acttcattgc 1980 aggtgcaagt tgcctacacc caataccagg gatttcaaga gtcaagagaa agtacagtaa 2040 acactattat cttatcttga ctttaagggg aaataatttc tcagaggatt ataattgtca 2100 ccgaagcctt aaatccttct gtcttcctga ctgaatgaaa cttgaattgg cagagcattt 2160 tccttatgga agggatgaga ttcccagaga cctgcattgc tttctcctgg ttttatttaa 2220 caatcgacaa atgaaattct tacagcctga aggcagacgt gtgcccagat gtgaaagaga 2280 ccttcagtat cagccctaac tcttctctcc caggaaggac ttgctgggct ctgtggccag 2340 ctgtccagcc cagccctgtg tgtgaatcgt ttgtgacgtg tgcaaatggg aaaggagggg 2400 tttttacatc tcctaaagga cctgatgcca acacaagtag gattgactta aactcttaag 2460 cgcagcatat tgctgtacac atttacagaa tggttgctga gtgtctgtgt ctgatttttt 2520 catgctggtc atgacctgaa ggaaatttat tagacgtata atgtatgtct ggtgttttta 2580 acttgatcat gatcagctct gaggtgcaac ttcttcacat actgtacata cctgtgacca 2640 ctcttgggag tgctgcagtc tttaatcatg ctgtttaaac tgttgtggca caagttctct 2700 tgtccaaata aaatttatta ataagatcta tagagagaga tatatacact tttgattgtt 2760 ttctagatgt ctaccaataa atgcaatttg tgacctgtat taatgattta aagtggggaa 2820 actagattaa aatatttgtc ttttaaaaaa aaaaaaaaaa aaaaaaaaaa aaaa 2874 <210> SEQ ID NO 196 <211> LENGTH: 609 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 196 Met Ser Val Glu Asn Lys Asn Arg Thr Arg Asp Gln Glu Ala Pro Glu 1 5 10 15 Asp Val Gln Val Arg Pro Glu Asp Thr Pro Ser Asp Leu Ser Val Ser 20 25 30 Asn Ser Ser Val Ile Leu Glu Asn Thr Met Glu Asp His Ala Ala Glu 35 40 45 Ala Ser Gly Lys Pro Leu Gly Glu Ile Ser Val Pro Leu Asp Ser Ser 50 55 60 Leu Leu Cys Thr Leu Ser Ser Glu Ser His Gln Glu Ala Ala Ser Asn 65 70 75 80 Glu Asn Asp Lys Lys Pro Gly Asn Tyr Lys Ser Met Leu Arg Pro Glu 85 90 95 Val Gly Thr Thr Ser Gln Asp Ser Ala Leu Leu Asp Gln Glu Leu Tyr 100 105 110 Asn Ser Phe His Phe Trp Arg Thr Pro Leu Pro Glu Ile Asp Leu Asp 115 120 125 Ile Glu Leu Glu Gln Asn Ser Gly Gly Lys Pro Ser Pro Glu Gly Pro 130 135 140 Glu Glu Glu Ser Glu Gly Pro Val Pro Ser Ser Pro Asn Ile Thr Met 145 150 155 160 Ala Thr Arg Lys Glu Leu Glu Glu Met Ile Glu Asn Leu Glu Pro His 165 170 175 Ile Asp Asp Pro Asp Val Lys Ala Gln Val Glu Val Leu Ser Ala Ala 180 185 190 Leu Arg Ala Ser Ser Leu Asp Ala His Glu Glu Thr Ile Ser Ile Glu 195 200 205 Lys Arg Ser Asp Leu Gln Asp Glu Leu Asp Ile Asn Glu Leu Pro Asn 210 215 220 Cys Lys Ile Asn Gln Glu Asp Ser Val Pro Leu Ile Ser Asp Ala Val 225 230 235 240 Glu Asn Met Asp Ser Thr Leu His Tyr Ile His Ser Asp Ser Asp Leu 245 250 255 Ser Asn Asn Ser Ser Phe Ser Pro Asp Glu Glu Arg Arg Thr Lys Val 260 265 270 Gln Asp Val Val Pro Gln Ala Leu Leu Asp Gln Tyr Leu Ser Met Thr 275 280 285 Asp Pro Ser Arg Ala Gln Thr Val Asp Thr Glu Ile Ala Lys His Cys 290 295 300 Ala Tyr Ser Leu Pro Gly Val Ala Leu Thr Leu Gly Arg Gln Asn Trp 305 310 315 320 His Cys Leu Arg Glu Thr Tyr Glu Thr Leu Ala Ser Asp Met Gln Trp 325 330 335 Lys Val Arg Arg Thr Leu Ala Phe Ser Ile His Glu Leu Ala Val Ile 340 345 350 Leu Gly Asp Gln Leu Thr Ala Ala Asp Leu Val Pro Ile Phe Asn Gly 355 360 365 Phe Leu Lys Asp Leu Asp Glu Val Arg Ile Gly Val Leu Lys His Leu 370 375 380 His Asp Phe Leu Lys Leu Leu His Ile Asp Lys Arg Arg Glu Tyr Leu 385 390 395 400 Tyr Gln Leu Gln Glu Phe Leu Val Thr Asp Asn Ser Arg Asn Trp Arg 405 410 415 Phe Arg Ala Glu Leu Ala Glu Gln Leu Ile Leu Leu Leu Glu Leu Tyr 420 425 430 Ser Pro Arg Asp Val Tyr Asp Tyr Leu Arg Pro Ile Ala Leu Asn Leu 435 440 445 Cys Ala Asp Lys Val Ser Ser Val Arg Trp Ile Ser Tyr Lys Leu Val 450 455 460 Ser Glu Met Val Lys Lys Leu His Ala Ala Thr Pro Pro Thr Phe Gly 465 470 475 480 Val Asp Leu Ile Asn Glu Leu Val Glu Asn Phe Gly Arg Cys Pro Lys 485 490 495 Trp Ser Gly Arg Gln Ala Phe Val Phe Val Cys Gln Thr Val Ile Glu 500 505 510 Asp Asp Cys Leu Pro Met Asp Gln Phe Ala Val His Leu Met Pro His 515 520 525 Leu Leu Thr Leu Ala Asn Asp Arg Val Pro Asn Val Arg Val Leu Leu 530 535 540 Ala Lys Thr Leu Arg Gln Thr Leu Leu Glu Lys Asp Tyr Phe Leu Ala 545 550 555 560 Phe Ala Ser Cys His Gln Glu Ala Val Glu Gln Thr Ile Met Ala Leu 565 570 575 Gln Met Asp Arg Asp Ser Asp Val Lys Tyr Phe Ala Ser Ile His Pro 580 585 590 Ala Ser Thr Lys Ile Ser Glu Asp Ala Met Ser Thr Ala Ser Ser Thr 595 600 605 Tyr <210> SEQ ID NO 197 <211> LENGTH: 2029 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 197 agcagccgaa tcttgagact gtcaatgaca gaaagctgaa gagaggcctc tatttcttcc 60 tttttccttt cttctgtcta aaaactctct cttgttcccc ttttccagct tcccttggac 120 tactgcccca atggcccctt ggactcgcgt ttcatgtatg cgagcacaca cacacacaaa 180 cttgcaaaat accgtttttc ttaaggattg tgggaccgaa taatatcacg tgccttcatc 240 ttttcctttt atagttagat gaacctcttc ctctttacaa tttttttaaa aagtgatagg 300 ggaggttgat gtgttagtgg aagatttggg catcgtttga gaagtaactt ttgtttaaca 360 cattccccct aaacattgaa cacaaacatt tcaacccctt catgacactc tttggacatt 420 taaagcattg agtaaccatg tacatgacag cctaaatccg tttgatttca gagcatttcc 480 tgaacattgt atttcataga cttctctgat tttttcaaaa atgaggtgag caatggcaag 540 cagccttgtt ctcccaattt ggtgcttttg cttttggtgt ggggtgggca tggggggttg 600 ggggtggtgt gggtgtgttt agaaaaaaga tgcattcctg aagatctctg gtgctgaagg 660 gcctcgagtt cctttcagag actgtatttg acacacttta ggtacacaca aacgaatggt 720 atcacatgca atattttaat ggagcaatgg gagaggctct ttgaaatggg gtttgcatct 780 ttttgtaaca ttatgatttc tctggtgcct tattcctact tgatgctggc actcacatac 840 ccacaagaag ctgacacaga agtcagcctt aggcgtgggg acatatgggt gatgtttgag 900 catgcagggg ccatggggag tttggtgtca gatggtggag aagggactag atggcatctc 960 ttagccgagg ccaacaggaa ctgcacaagt ccattatagt caaagttagc aattttgata 1020 cgtaaacaca atacttcatt cttcctcatc tgagctttcc ttccttcttc cttttctatc 1080 tctaccttct cataaaggtg ctgctgctgc tgctaaggtg cccggagtcc agaatgtcca 1140 ttaatcactc aggcacgagc ctggcactgc cacgtcagcc cccagcatga ccaaacccag 1200 gtttctcttg cttggggctg agaactgtca gatttttctc atcaaaaatg ttttccaagg 1260 aatcagtgga ttacagtttt tctgcattga aaatgcactt taaaaaataa attaaagctc 1320 cagactgttt aaaatataca gagggagcag gggaaagtta agcatgtgct agtgtctgaa 1380 cccagttcag tttatctcca gttgaaacga tatacactat attatgtata aatgtataca 1440 cacttcctat atgtatccac atatatatag tgtatatatt atacatgtat aggtgtgtat 1500 atgtgcatat atacacacat gcacataaca aaatcagatg ctcattacaa atccagatgc 1560 tcattacaaa accagatgct acacaaacag cagcagagga aacaaggttg gactcttgca 1620 acagatcaca aaaaataaaa acagctactt gcagtgactt tggtcatttc tgtatgttca 1680 taaagaatgg attgtaacaa ggaaaaaaag gaacagtgtt agtgaaaaag gaaaaatggg 1740 cgaaaccatc ttgatccgat gcgaatgcag taatgttcta tataccattt catcagttat 1800 ttcttttagt catgttgatt tgatttcagt ttctggctat gaaaaacatt tttaaactcg 1860 tcacccacaa caaactgaac aaaactacta cagtgaaagc ccttttcagt gaaagatgtc 1920 agaaacctca aaacctttgg cctgactcag aactaccatg tgaaaatcag tactctctta 1980 atgtttgaaa taaaaactga aaaaaaaaaa aaaaaaaaaa aaaaaaaaa 2029 <210> SEQ ID NO 198 <211> LENGTH: 86 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 198 Met Glu Gln Trp Glu Arg Leu Phe Glu Met Gly Phe Ala Ser Phe Cys 1 5 10 15 Asn Ile Met Ile Ser Leu Val Pro Tyr Ser Tyr Leu Met Leu Ala Leu 20 25 30 Thr Tyr Pro Gln Glu Ala Asp Thr Glu Val Ser Leu Arg Arg Gly Asp 35 40 45 Ile Trp Val Met Phe Glu His Ala Gly Ala Met Gly Ser Leu Val Ser 50 55 60 Asp Gly Gly Glu Gly Thr Arg Trp His Leu Leu Ala Glu Ala Asn Arg 65 70 75 80 Asn Cys Thr Ser Pro Leu 85 <210> SEQ ID NO 199 <211> LENGTH: 2304 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 199 cagggtctgg ccactgcaca gccaggcacg ctggctgctg tggcagggtg ggaagctcca 60 tatgccagct ccctttgagg ctgcggctgg accagatgtg ccacaagtgg cttccactgt 120 gggcaccagc gtctggataa agggaatgtg gtggtgcccg aaagctcaga gacaccagga 180 actgcagagt ccccaaatag gtgttacagc atgtcacagc catggctcag ggagcaccaa 240 ggtctgggct tccagaaggg ctgcagctct tctctacttc ttgttatcta cagtgtggtg 300 agtgggggga catgtttcag cccatttgtg ttacagctct ttcagtccca ccaccttgct 360 ctggcccgtg gctcatgggc tggaccagcc ccactgctgc ttcccatcat gtggggtggc 420 cactcagcac cagcagaggg tgggagggct atagtgttaa cagcagctcc agctctgagg 480 tctgggcccc cagaagggtt gccatccttt actcccatag cccaggagca tgtcaccacc 540 cacagctcag cgagctggtc aagaacatgt tacagctcct ttcacttccg ccgttcagca 600 ggtcctgagt tcttgtcccg tgtctaggaa gaatgaggtt atgcagacaa ctgggtgaac 660 aaggcaggca ggagctttat tgagtgacag aacagctgtc aggagaccca aagtgggtag 720 ctcctttcta caggtggtcc agacaagtgt cttaggctgg ctgagtctgg ggtttttaag 780 ggctcagaag ggaggaaggg catgctgatt ggtccatagg tggtcatagg caggcctgga 840 aaaagcacca tctgattggc aaaaggcatc agtgaagttc tcactccagg ttgcggactc 900 cacctggaac ggacagctga gcccccaggc ttcaggccat ccctggctta aaggtagggt 960 ttcactagag acccacccct tcctgcctag gaacctgtct gcctcccact gccatcaaca 1020 tgccatccat ggcacccagg ctatctgcac tgaggggcac ccacatgccc acgctcagct 1080 gccctcaatg cccccagcct ccctcccaca ctcatcactg cccgaagtcc agaaagggct 1140 gaggcagcag ggtgctgggt ctgccacaac tttgcttcgc actggagcgg gcacttggag 1200 agaggagagg ccagagagtg ggaacaggca cctctgcctg aaggaatagg gggcttccca 1260 ggccctggag agtgcaggga tgcccaggtc cacagctggg cagctgcaac tgcctgggag 1320 aacaggctcc catcctgcca gcttggtagg gcgcagggct cctgctggga tcacctattc 1380 ctggcccctg ccagctccac agagtgcaca atcccagcca tggcttcccc cactgcagct 1440 ggcgtcctca cagcagccac cccagatggg ccactgctgc tgtcaacagt tggcaggaag 1500 gcaggctaag cctggtgtct caaccagagg actttgcagc agaggtaatt gccaacccca 1560 cttccactgc cttgacgtcc ctcttgcagc agagaagcta atcctgccca gcctggccat 1620 gagtgagggc acctgaaggg gtgaggaggc gggggtaatg ttgtgtaggt gggagggggc 1680 agtagagagt cccatactca aagtgactgc caaatccagg gctgtgcata gagtgactgc 1740 tgacagcctt tgataagctt tgctgtgagt ccaaaagaat gatcggatag atgcctgtct 1800 tgcagcgcat ctacattaat ctcatagcaa attattcgtc tcatattaga gaaagtttag 1860 ctttcttaga agcttgatgg gaaagagcct cccagctctt agagtttgat tttcgcaact 1920 cagttcacat cttcttctta ctccaggttc ccagctcctt gagccttgcc cgtgaagggg 1980 ttggagtcag gatgggaagc cttgagctgc cttgacctgc tccatctctg actcagggat 2040 gtgccctgct tgtcacagca tgggtgtgct gggccttggg gcatcttttc aggcagagag 2100 caagacgttg gcattgtgga aagctgtccc tccaaacagc agcccattca cagactacag 2160 aggaagaaaa gaccacactt gctacagtaa caatgcaatt cagtaccagg gaataactta 2220 acatgaaaca tgtcaaatct atgtaaacaa ctggaaggca ctcctaaaaa atacaaaaaa 2280 aaaaaaaaaa aaaaaaaaaa aaaa 2304 <210> SEQ ID NO 200 <211> LENGTH: 128 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 200 Met Ala Gln Gly Ala Pro Arg Ser Gly Leu Pro Glu Gly Leu Gln Leu 1 5 10 15 Phe Ser Thr Ser Cys Tyr Leu Gln Cys Gly Glu Trp Gly Asp Met Phe 20 25 30 Gln Pro Ile Cys Val Thr Ala Leu Ser Val Pro Pro Pro Cys Ser Gly 35 40 45 Pro Trp Leu Met Gly Trp Thr Ser Pro Thr Ala Ala Ser His His Val 50 55 60 Gly Trp Pro Leu Ser Thr Ser Arg Gly Trp Glu Gly Tyr Ser Val Asn 65 70 75 80 Ser Ser Ser Ser Ser Glu Val Trp Ala Pro Arg Arg Val Ala Ile Leu 85 90 95 Tyr Ser His Ser Pro Gly Ala Cys His His Pro Gln Leu Ser Glu Leu 100 105 110 Val Lys Asn Met Leu Gln Leu Leu Ser Leu Pro Pro Phe Ser Arg Ser 115 120 125 <210> SEQ ID NO 201 <211> LENGTH: 1458 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (493) <400> SEQUENCE: 201 gggccatggt tccctgcggg cggcggggag ggatttcctg gggcgccccc tggaatccaa 60 gcccgaccgc agtgtctgac catggtccgc ggcgcggccg ggtggtcctg caggggccgc 120 gcatagctcc gactacagca tgtggaggaa gaaccagtac gtcagtaacg ggctgcgcga 180 ctttgcggag cgcggcgagg cctgggcgct gatgaaggag atcgaggcgg cgggggaggc 240 gctgcagagc gtgcacgcgg tgttttcggc gcccgccgtc cccagcggca ccgggcagac 300 gtcggcggag ctggaggtgc agcgcaggca ctcgctggtc tcgtttgtgg tgcgcatcgt 360 gcccagcccc gactggttcg tgggcgtgaa cagcctggac ctgtgcgacg gggaccgttg 420 gcgggaacag gcggcgctgg acctgtaccc ctacgacgcc gggacggaca gcggcttcac 480 cttctcctcc ccnaacttcg ccaccatccc gcaggacacg gtgaccgaga taacgtcctc 540 ctctcccagc cacccggcca actccttcta ctacccgcgg ctgaaggccc tgcctcccat 600 cgccagggtg acactggtgc ggctgcgaca gagccccagg gccttcatcc ctcccgcccc 660 agtcctgccc agcagggaca atgagattgt agacagcgcc tcagttccag aaacgccgct 720 ggactgcgag gtctccctgt ggtcgtcctg gggactgtgc ggaggcccac tgtgggaggc 780 tcgggaccaa gagcaggact cgctacgtcc gggtccagcc cgccaacaaa cgggagcccc 840 tgccccgagc tcgaagaaga ggctgagtgc gtccctgata actgcgtcta agaccagagc 900 cccgcagccc ctggggcccc ccggagccat ggggtgtcgg gggctcctgt gcaggctcat 960 gctgcaggcg gccgagggca cagggggttt cgcgctgctc ctgaccgcgg tgaggccgcg 1020 ccgaccatct ctgcactgaa gggccctctg gtggccggca cgggcattgg gaaacagcct 1080 cctcctttcc caaccttgct tcttaggggc ccccgtgtcc cgtctgctct cagcctcctc 1140 ctcctgcagg ataaagtcat ccccaaggct ccagctactc taaattatgt ctccttataa 1200 gttattgctg ctccaggaga ttgtccttca tcgtccaggg gcctggctcc cacgtggttg 1260 cagatacctc agacctggtg ctctaggctg tgctgagccc actctcccga gggcgcatcc 1320 aagcgggggc cacttgagaa gtgaataaat ggggcggttt cggaagcgtc agtgtttcca 1380 tgttatggat ctctctgcgt ttgaataaag actatctctg ttgctcacaa aaaaaaaaaa 1440 aaaaaaaaaa aaaaaaaa 1458 <210> SEQ ID NO 202 <211> LENGTH: 299 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 202 Met Trp Arg Lys Asn Gln Tyr Val Ser Asn Gly Leu Arg Asp Phe Ala 1 5 10 15 Glu Arg Gly Glu Ala Trp Ala Leu Met Lys Glu Ile Glu Ala Ala Gly 20 25 30 Glu Ala Leu Gln Ser Val His Ala Val Phe Ser Ala Pro Ala Val Pro 35 40 45 Ser Gly Thr Gly Gln Thr Ser Ala Glu Leu Glu Val Gln Arg Arg His 50 55 60 Ser Leu Val Ser Phe Val Val Arg Ile Val Pro Ser Pro Asp Trp Phe 65 70 75 80 Val Gly Val Asn Ser Leu Asp Leu Cys Asp Gly Asp Arg Trp Arg Glu 85 90 95 Gln Ala Ala Leu Asp Leu Tyr Pro Tyr Asp Ala Gly Thr Asp Ser Gly 100 105 110 Phe Thr Phe Ser Ser Pro Asn Phe Ala Thr Ile Pro Gln Asp Thr Val 115 120 125 Thr Glu Ile Thr Ser Ser Ser Pro Ser His Pro Ala Asn Ser Phe Tyr 130 135 140 Tyr Pro Arg Leu Lys Ala Leu Pro Pro Ile Ala Arg Val Thr Leu Val 145 150 155 160 Arg Leu Arg Gln Ser Pro Arg Ala Phe Ile Pro Pro Ala Pro Val Leu 165 170 175 Pro Ser Arg Asp Asn Glu Ile Val Asp Ser Ala Ser Val Pro Glu Thr 180 185 190 Pro Leu Asp Cys Glu Val Ser Leu Trp Ser Ser Trp Gly Leu Cys Gly 195 200 205 Gly Pro Leu Trp Glu Ala Arg Asp Gln Glu Gln Asp Ser Leu Arg Pro 210 215 220 Gly Pro Ala Arg Gln Gln Thr Gly Ala Pro Ala Pro Ser Ser Lys Lys 225 230 235 240 Arg Leu Ser Ala Ser Leu Ile Thr Ala Ser Lys Thr Arg Ala Pro Gln 245 250 255 Pro Leu Gly Pro Pro Gly Ala Met Gly Cys Arg Gly Leu Leu Cys Arg 260 265 270 Leu Met Leu Gln Ala Ala Glu Gly Thr Gly Gly Phe Ala Leu Leu Leu 275 280 285 Thr Ala Val Arg Pro Arg Arg Pro Ser Leu His 290 295 <210> SEQ ID NO 203 <211> LENGTH: 1100 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 203 attacaggcg tgagccatgc gtccagcagg aaaaggtttt ttaatgaacc atagagacct 60 ctcagagctc cagatttggg ggatggggtc agataatcag gagagttccc gaagaaagtg 120 ccatttgagc tgtgatctga aggaacacta gtaagtagtc agctaggcac agatggggag 180 aggagagggc attctgggcc gaggacacag cgtgggtgaa atcctggagg tgggaagcgg 240 cactgtgctc cagagggact ggaggagagc cagagtgact ggcacatcag gagggcacag 300 gggatgcccg agctgctggt gagacagaca ggactgagag aaacagcaag ctggtctctg 360 acagcttccc gtcaagtggt gatctgtctc ccttcgtcct cccctgccct cccactatct 420 ctgttttccc cagtgccctt tctttccttt ccctgttctt ccttttggaa gaacatacga 480 gctcacctgt gttctggttc cttttctaaa gggctttatg attacttaac caacctcata 540 accatggacc agccaacatt tcacaaatac tcactcaaaa caagcctgtt attatcaccc 600 tcgtttcaca gaagtggaaa ctggggtgca gaaagatgaa gggtcagcag ctggtcagtg 660 acgagccagg gtccaaggcc aggatgtctg cccagccgcc atgctcactg cctttcatct 720 tggttctcct aggaagagtt agttacttct agggtattat tagattggtg caaaagtaat 780 tgtgggtttt gccattgaaa ataattactt ctacaccaac ctaatacttt tttcccaagg 840 ggtttagtag aaggattcct gcagaccaga aacccagagg gatattgctg atgtggtagg 900 tgttgggcca gcagggagag aggtctgagc ccctgccagg tgctacctgg gagccacttt 960 gtcagcattt gtttgttcta cttgggaggt agccctgcca gggacacctg gggacacctt 1020 ttcccactgg aagcgccatc tgaatccaga accgttttct ttgtcttaag aaaaaaaaaa 1080 aaaaaaaaaa aaaaaaaaaa 1100 <210> SEQ ID NO 204 <211> LENGTH: 111 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 204 Met Pro Glu Leu Leu Val Arg Gln Thr Gly Leu Arg Glu Thr Ala Ser 1 5 10 15 Trp Ser Leu Thr Ala Ser Arg Gln Val Val Ile Cys Leu Pro Ser Ser 20 25 30 Ser Pro Ala Leu Pro Leu Ser Leu Phe Ser Pro Val Pro Phe Leu Ser 35 40 45 Phe Pro Cys Ser Ser Phe Trp Lys Asn Ile Arg Ala His Leu Cys Ser 50 55 60 Gly Ser Phe Ser Lys Gly Leu Tyr Asp Tyr Leu Thr Asn Leu Ile Thr 65 70 75 80 Met Asp Gln Pro Thr Phe His Lys Tyr Ser Leu Lys Thr Ser Leu Leu 85 90 95 Leu Ser Pro Ser Phe His Arg Ser Gly Asn Trp Gly Ala Glu Arg 100 105 110 <210> SEQ ID NO 205 <211> LENGTH: 1395 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 205 ttcaagacca gcctgaccaa catggagaaa ccctgtctct actaaaaata caaaattagc 60 cgggcatggt ggcaatgcct gcctgtaatc ccagctactc gggaggctga ggcaaaagaa 120 tcgcttgaac ccaggaggca gaggttgcag tgagctgaga ttgtgctatt gcactccagc 180 ctggataaca agagcgagac tccgtctcaa aaaaaaaaaa aaatttgtag agatagtgtt 240 ttgctacgtt actcagggtg gtctcaaact cctggcctca ggcagttctg cctaggcttc 300 ccaaagtact gggattacag gcagaagcca ctgcgcctac catagaatat tagttatctt 360 ttgaagtgat taaaaaggga aaagattttc ttccaagttt aatgatgaga aaagtgaaag 420 aacagttatt ttaaagcccc tgatatttcc aacatctagg tcataaatga gtctcgttct 480 gttgatagct ttatctcttg gtaatgtgca tgcctgtgtg tgtgtgtgtg tgtgtgttct 540 attctgtgat gtcttataat ttttagttta atggcaaaca tcatgtatac aagaccagta 600 gagactgagg tagatggtat tctgtgtctg gatataggca cgcctctccc atcaggccaa 660 ttgcctgtga cattgagtca acctagtctg gagttgaggt ggatttggat tttgatgttg 720 gtatcattat gttcagtgta cttgggctgc tgttacctgg tacctggagc ctggggtacc 780 agatggtttt tcttcagtgt ttctgttcca ctgttggctt tcctcagtcc catcatgcct 840 ccatcacaga gggggagtct ctattcatat ccttgcccct tcactagtgg ttgactgatg 900 ctgcttgtta ctcagtgcta ggcttatggt ggtgtcatag gtggttttct attgtcctgg 960 ttcagcctta gctttaggca gtccctgttc atttgaaccc caggggtggt acttaatctg 1020 ccctttcctg agcagtagca aacctctgct tggcatcaga ttcttgggcc aatgaggatt 1080 ctctcctgct ctcccagaaa caagatgttt gcttctacct ctcccccagc agcaataggg 1140 tatgtgagag gtgggaggtt tacttgaacc caggaggtcg aggctgcagt gagccatgat 1200 agtggcacca cactccagcc tgggtgacag agcaagaccc tgtctcaaaa caacaacaac 1260 aacccaaaaa actgtcaagg tcatcaggaa caaaacatag ccaatagcca agaaactgtc 1320 acataccaga ggagactaag gaaacatgat gactaaatgc aatacaaaaa aaaaaaaaaa 1380 aaaaaaaaaa aaaaa 1395 <210> SEQ ID NO 206 <211> LENGTH: 107 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 206 Met Ala Asn Ile Met Tyr Thr Arg Pro Val Glu Thr Glu Val Asp Gly 1 5 10 15 Ile Leu Cys Leu Asp Ile Gly Thr Pro Leu Pro Ser Gly Gln Leu Pro 20 25 30 Val Thr Leu Ser Gln Pro Ser Leu Glu Leu Arg Trp Ile Trp Ile Leu 35 40 45 Met Leu Val Ser Leu Cys Ser Val Tyr Leu Gly Cys Cys Tyr Leu Val 50 55 60 Pro Gly Ala Trp Gly Thr Arg Trp Phe Phe Phe Ser Val Ser Val Pro 65 70 75 80 Leu Leu Ala Phe Leu Ser Pro Ile Met Pro Pro Ser Gln Arg Gly Ser 85 90 95 Leu Tyr Ser Tyr Pro Cys Pro Phe Thr Ser Gly 100 105 <210> SEQ ID NO 207 <211> LENGTH: 1617 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 207 tccacttatt ctggatattc ttactattca agtcattcga aaaaatctca cagacaaggg 60 gaaagaacta gagagagaca caagtcaccc cggaataaag acggcagagg gtcagaaaag 120 tctgtcacca ttcaacctcc cactggagag cccctgttgg gaaatgattc tactcggaca 180 gaggaagttc aggatgacaa ctggggagag accaccacgg ccatcacagg cacctcggag 240 cacagcatat cccaagagga cattgccagg atcagcaagg acatggagga cagcgtgggg 300 ctggattgca aacgctacct gggcctcacc gtcgcctctt ttcttggact tctagttttc 360 ctcaccccta ttgccttcat ccttttacct ccgatcctgt ggagggatga gctggagcct 420 tgtggcacaa tttgtgaggg gctctttatc tccatggcat tcaaactcct cattctgctc 480 atagggacct gggcactttt tttccgcaag cggagagctg acatgccacg ggtgtttgtg 540 tttcgtgccc ttttgttggt cctcattttt ctctttgtgg tttcctattg gcttttttac 600 ggggtccgca ttttggactc tcgggaccgg aattaccagg gcattgtgca atatgcagtc 660 tcccttgtgg atgccctcct cttcatccat tacctggcca tcgtcctgct ggagctcagg 720 cagctgcagc ccatgttcac gctgcaggtg gtccgctcca ccgatggcga gtcccgcttc 780 tacagcctgg gacacctgag tatccagcga gcagcattgg tggtcctaga aaattactac 840 aaagatttca ccatctataa cccaaacctc ctaacagcct ccaaattccg agcagccaag 900 catatggccg ggctgaaagt ctacaatgta gatggcccca gtaacaatgc cactggccag 960 tcccgggcca tgattgctgc agctgctcgg cgcagggact caagccacaa cgagttgtat 1020 tatgaagagg ccgaacatga acggcgagta aagaagcgga aagcaaggct ggtggttgca 1080 gtggaagagg ccttcatcca cattcagcgt ctccaggctg aggagcagca gaaagcccca 1140 ggggaggtga tggaccctag ggaggccgcc caggccattt tcccctccat ggccagggct 1200 ctccagaagt acctgcgcat cacccggcag cagaactacc acagcatgga gagcatcctg 1260 cagcacctgg ccttctgcat caccaacggc atgaccccca aggccttcct agaacggtac 1320 ctcagtgcgg gccccaccct gcaatatgac aaggaccgct ggctctctac acagtggagg 1380 cttgtcagtg atgaggctgt gactaatgga ttacgggatg gaattgtgtt cgtccttaag 1440 tgcttggact tcagcctcgt agtcaatgtg aagaaaattc cattcatcat actctctgaa 1500 gagttcatag accccaaatc tcacaaattt gtccttcgct tacagtctga gacatccgtt 1560 taaaagttct atatttgtgg ctttattaaa aaaaaaaaaa aaaaaaaaaa aaaaaaa 1617 <210> SEQ ID NO 208 <211> LENGTH: 426 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 208 Met Glu Asp Ser Val Gly Leu Asp Cys Lys Arg Tyr Leu Gly Leu Thr 1 5 10 15 Val Ala Ser Phe Leu Gly Leu Leu Val Phe Leu Thr Pro Ile Ala Phe 20 25 30 Ile Leu Leu Pro Pro Ile Leu Trp Arg Asp Glu Leu Glu Pro Cys Gly 35 40 45 Thr Ile Cys Glu Gly Leu Phe Ile Ser Met Ala Phe Lys Leu Leu Ile 50 55 60 Leu Leu Ile Gly Thr Trp Ala Leu Phe Phe Arg Lys Arg Arg Ala Asp 65 70 75 80 Met Pro Arg Val Phe Val Phe Arg Ala Leu Leu Leu Val Leu Ile Phe 85 90 95 Leu Phe Val Val Ser Tyr Trp Leu Phe Tyr Gly Val Arg Ile Leu Asp 100 105 110 Ser Arg Asp Arg Asn Tyr Gln Gly Ile Val Gln Tyr Ala Val Ser Leu 115 120 125 Val Asp Ala Leu Leu Phe Ile His Tyr Leu Ala Ile Val Leu Leu Glu 130 135 140 Leu Arg Gln Leu Gln Pro Met Phe Thr Leu Gln Val Val Arg Ser Thr 145 150 155 160 Asp Gly Glu Ser Arg Phe Tyr Ser Leu Gly His Leu Ser Ile Gln Arg 165 170 175 Ala Ala Leu Val Val Leu Glu Asn Tyr Tyr Lys Asp Phe Thr Ile Tyr 180 185 190 Asn Pro Asn Leu Leu Thr Ala Ser Lys Phe Arg Ala Ala Lys His Met 195 200 205 Ala Gly Leu Lys Val Tyr Asn Val Asp Gly Pro Ser Asn Asn Ala Thr 210 215 220 Gly Gln Ser Arg Ala Met Ile Ala Ala Ala Ala Arg Arg Arg Asp Ser 225 230 235 240 Ser His Asn Glu Leu Tyr Tyr Glu Glu Ala Glu His Glu Arg Arg Val 245 250 255 Lys Lys Arg Lys Ala Arg Leu Val Val Ala Val Glu Glu Ala Phe Ile 260 265 270 His Ile Gln Arg Leu Gln Ala Glu Glu Gln Gln Lys Ala Pro Gly Glu 275 280 285 Val Met Asp Pro Arg Glu Ala Ala Gln Ala Ile Phe Pro Ser Met Ala 290 295 300 Arg Ala Leu Gln Lys Tyr Leu Arg Ile Thr Arg Gln Gln Asn Tyr His 305 310 315 320 Ser Met Glu Ser Ile Leu Gln His Leu Ala Phe Cys Ile Thr Asn Gly 325 330 335 Met Thr Pro Lys Ala Phe Leu Glu Arg Tyr Leu Ser Ala Gly Pro Thr 340 345 350 Leu Gln Tyr Asp Lys Asp Arg Trp Leu Ser Thr Gln Trp Arg Leu Val 355 360 365 Ser Asp Glu Ala Val Thr Asn Gly Leu Arg Asp Gly Ile Val Phe Val 370 375 380 Leu Lys Cys Leu Asp Phe Ser Leu Val Val Asn Val Lys Lys Ile Pro 385 390 395 400 Phe Ile Ile Leu Ser Glu Glu Phe Ile Asp Pro Lys Ser His Lys Phe 405 410 415 Val Leu Arg Leu Gln Ser Glu Thr Ser Val 420 425 <210> SEQ ID NO 209 <211> LENGTH: 2259 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (2194) <400> SEQUENCE: 209 ccaaagaggc ctagacactt tgggggtgca ctggcacttt gcagggttca ctggcacttt 60 ctggggctca ttgacacttt ggggtacact ggcattcttt ggtgttcact ggcattttgg 120 gggtgcactg gcactttgga acaacggcac gcctcttggc ccttgcccag ctggtgctcc 180 tggctgggaa gctgaacaca ctggctgctg tggtcactgt cttctacctg gtggcctatg 240 ctgccgtgga cctgtcctgc ctgagcctgg agtgggcctc ggccccaact tccggtgaga 300 gactcagatc tgtgtcccca gagagaagaa gggaggactc gggctcaggc gtggggctgg 360 ggactgcagc ctcgtgtgcg gcctgccctg agtttctgtc cctcctcccc tccatgcccg 420 tagccccacc ttcagcctgt tctcctggca cacctgcctg ctgggggtgg cctcctgcct 480 gctcatgatg ttcctcatca gtcctggcgc ggctggtggc tccctgctcc tcatgggtct 540 gctggctgcc ctgctcaccg cgcgaggagg ccccagtagc tggggctatg tcagccaggc 600 cttgcttttc caccaggtgc gtaagtatct gcttcggctg gacgtccgga aggatcacgt 660 gaagttctgg cggccccagc tgctgctcct ggtggggaac ccccggggcg ccctgcctct 720 gctgcggttg gccaaccagc ttaagaaggg ggggctgtat gtgctgggcc acgtcaccct 780 gggagacctc gactccctgc cctcggaccc tgtacagccg cagtatgggg catggctcag 840 cctggtggac cgtgcccagg tgaaggcttt tgtggatcta accctctcac cctccgtgcg 900 ccagggggct cagcatctgc tgcgaatctc cggcctcggt ggcatgaagc ccaacacgtt 960 ggtcctaggt ttctacgatg acgctccacc gcaggaccat ttcctgacgg acccggcttt 1020 ctctgagcct gcagacagca ccagggaggg cagttcccca gctctgagca ccctgttccc 1080 tcctccccgg gctcctggga gcccccgggc cctcaatccc caggactatg tggccacggt 1140 ggccgacgcc ctcaagatga acaagaatgt ggtgctggcc cgggccagcg gggccttgcc 1200 ccctgagcgg ctgagccggg ggtctggggg cacctctcag ctgcaccatg tggacgtgtg 1260 gccctcaacc tgctgcggcc ccggggtggg cccggctatg tggatgtctg cggcctcttc 1320 ctgctgcaga tggcaaccat cttgggcatg gtgcccgctt ggcatagcgc ccggctccgg 1380 atcttcctgt gcctggggcc tcgggaggcg cctggggcgg ccgagggcgg ctgcgggcac 1440 tgctgagcca actgaggatc cgggctgagg tgcagaaggt ggtgtggggc gagggggccg 1500 gggctgggga acccgaggcg gaggaggaag gggactttgt gaacagtggg cggggagacg 1560 cagaggcaga ggccctggca cgcagcgcca acgccctggt tcgggcccag caggggcgcg 1620 gcacaggagg agggccgggt gggccggagg gtggggatgc tgagggcccc atcacagccc 1680 tcaccttcct gtacttgcct cggccgccag ccgatcccgc ccgatacccc cgctacctgg 1740 cgctactgga gactctaacc cgagacctgg gccccacgct gctggttcat ggggtcactc 1800 cagtcacctg cactgatctg tgatgcccct gcctccaggg ctaggtagag agggcccagg 1860 caggcggcct atcctgatcc ttggaggagg tggaagagga ggccactgtg gcccgtggcc 1920 ctgcccttgg gacgtggagc ccaggggagg tttgaagggg atcctgggct tgggcatcac 1980 gcccacctcc tttggcagag ggaccccagc acactaactc tgggtggctg tccccaccgt 2040 gcgggggggg gagtccgcag cctcccttca ctggtgcctt gatgctgggg gccaggcctc 2100 ctctgtgact ctgggctccc tcagtttccc cattttggcc agactcaccg gcccactggg 2160 gtggtgatgt tttcgttctg ttttattttt ctanctctgc tgaccatgaa taaaagacca 2220 aaacactatt aaaaaaaaaa aaaaaaaaaa aaaaaaaaa 2259 <210> SEQ ID NO 210 <211> LENGTH: 327 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 210 Met Met Phe Leu Ile Ser Pro Gly Ala Ala Gly Gly Ser Leu Leu Leu 1 5 10 15 Met Gly Leu Leu Ala Ala Leu Leu Thr Ala Arg Gly Gly Pro Ser Ser 20 25 30 Trp Gly Tyr Val Ser Gln Ala Leu Leu Phe His Gln Val Arg Lys Tyr 35 40 45 Leu Leu Arg Leu Asp Val Arg Lys Asp His Val Lys Phe Trp Arg Pro 50 55 60 Gln Leu Leu Leu Leu Val Gly Asn Pro Arg Gly Ala Leu Pro Leu Leu 65 70 75 80 Arg Leu Ala Asn Gln Leu Lys Lys Gly Gly Leu Tyr Val Leu Gly His 85 90 95 Val Thr Leu Gly Asp Leu Asp Ser Leu Pro Ser Asp Pro Val Gln Pro 100 105 110 Gln Tyr Gly Ala Trp Leu Ser Leu Val Asp Arg Ala Gln Val Lys Ala 115 120 125 Phe Val Asp Leu Thr Leu Ser Pro Ser Val Arg Gln Gly Ala Gln His 130 135 140 Leu Leu Arg Ile Ser Gly Leu Gly Gly Met Lys Pro Asn Thr Leu Val 145 150 155 160 Leu Gly Phe Tyr Asp Asp Ala Pro Pro Gln Asp His Phe Leu Thr Asp 165 170 175 Pro Ala Phe Ser Glu Pro Ala Asp Ser Thr Arg Glu Gly Ser Ser Pro 180 185 190 Ala Leu Ser Thr Leu Phe Pro Pro Pro Arg Ala Pro Gly Ser Pro Arg 195 200 205 Ala Leu Asn Pro Gln Asp Tyr Val Ala Thr Val Ala Asp Ala Leu Lys 210 215 220 Met Asn Lys Asn Val Val Leu Ala Arg Ala Ser Gly Ala Leu Pro Pro 225 230 235 240 Glu Arg Leu Ser Arg Gly Ser Gly Gly Thr Ser Gln Leu His His Val 245 250 255 Asp Val Trp Pro Ser Thr Cys Cys Gly Pro Gly Val Gly Pro Ala Met 260 265 270 Trp Met Ser Ala Ala Ser Ser Cys Cys Arg Trp Gln Pro Ser Trp Ala 275 280 285 Trp Cys Pro Leu Gly Ile Ala Pro Gly Ser Gly Ser Ser Cys Ala Trp 290 295 300 Gly Leu Gly Arg Arg Leu Gly Arg Pro Arg Ala Ala Ala Gly Thr Ala 305 310 315 320 Glu Pro Thr Glu Asp Pro Gly 325 <210> SEQ ID NO 211 <211> LENGTH: 1001 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: (812) <400> SEQUENCE: 211 gaaaccgttg atgggactga gaaaccagag ttaaaacctc tttggagctt ctgaggactc 60 agctggaacc aacgggcaca gttggcaaca ccatcatgac atcacaacct gttcccaatg 120 agaccatcat agtgctccca tcaaatgtca tcaacttctc ccaagcagag aaacccgaac 180 ccaccaacca ggggcaggat agcctgaaga aacatctaca cgcagaaatc aaagttattg 240 ggactatcca gatcttgtgt ggcatgatgg tattgagctt ggggatcatt ttggcatctg 300 cttccttctc tccaaatttt acccaagtga cttctacact gttgaactct gcttacccat 360 tcataggacc cttttttttt atcatctctg gctctctatc aatcgccaca gagaaaaggt 420 taaccaagct tttggtgcat agcagcctgg ttggaagcat tctgagtgct ctgtctgccc 480 tggtgggttt cattatcctg tctgtcaaac aggccacctt aaatcctgcc tcactgcagt 540 gtgagttgga caaaaataat ataccaacaa gaagttatgt ttcttacttt tatcatgatt 600 cactttatac cacggactgc tatacagcca aagccagtct ggctggaact ctctctctga 660 tgctgatttg cactctgctg gaattctgcc ttgctgtgct cactgctgtg ctgcggtgga 720 aacaggctta ctctgacttc cctgggagtg tacttttcct gcctcacagt tacattggta 780 attctggcat gtcctcaaaa atgactcatg anctgtggat atgaagaact attgacttct 840 taagaaaaaa gggagaaata ttaatcagaa agttgattct tatgataata tggaaaagtt 900 aaccattata gaaaagcaaa gcttgagttt cctaaatgta agcttttaaa gtaatgaaca 960 ttaaaaaaaa ccattatttc actgtcaaaa aaaaaaaaaa a 1001 <210> SEQ ID NO 212 <211> LENGTH: 242 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: UNSURE <222> LOCATION: (239) <400> SEQUENCE: 212 Met Thr Ser Gln Pro Val Pro Asn Glu Thr Ile Ile Val Leu Pro Ser 1 5 10 15 Asn Val Ile Asn Phe Ser Gln Ala Glu Lys Pro Glu Pro Thr Asn Gln 20 25 30 Gly Gln Asp Ser Leu Lys Lys His Leu His Ala Glu Ile Lys Val Ile 35 40 45 Gly Thr Ile Gln Ile Leu Cys Gly Met Met Val Leu Ser Leu Gly Ile 50 55 60 Ile Leu Ala Ser Ala Ser Phe Ser Pro Asn Phe Thr Gln Val Thr Ser 65 70 75 80 Thr Leu Leu Asn Ser Ala Tyr Pro Phe Ile Gly Pro Phe Phe Phe Ile 85 90 95 Ile Ser Gly Ser Leu Ser Ile Ala Thr Glu Lys Arg Leu Thr Lys Leu 100 105 110 Leu Val His Ser Ser Leu Val Gly Ser Ile Leu Ser Ala Leu Ser Ala 115 120 125 Leu Val Gly Phe Ile Ile Leu Ser Val Lys Gln Ala Thr Leu Asn Pro 130 135 140 Ala Ser Leu Gln Cys Glu Leu Asp Lys Asn Asn Ile Pro Thr Arg Ser 145 150 155 160 Tyr Val Ser Tyr Phe Tyr His Asp Ser Leu Tyr Thr Thr Asp Cys Tyr 165 170 175 Thr Ala Lys Ala Ser Leu Ala Gly Thr Leu Ser Leu Met Leu Ile Cys 180 185 190 Thr Leu Leu Glu Phe Cys Leu Ala Val Leu Thr Ala Val Leu Arg Trp 195 200 205 Lys Gln Ala Tyr Ser Asp Phe Pro Gly Ser Val Leu Phe Leu Pro His 210 215 220 Ser Tyr Ile Gly Asn Ser Gly Met Ser Ser Lys Met Thr His Xaa Leu 225 230 235 240 Trp Ile <210> SEQ ID NO 213 <211> LENGTH: 1079 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <400> SEQUENCE: 213 gcatcctcct ctatcctgtt tcgaggtaga gagcttggca cttctgttac aagctgagag 60 tctggaggtg ctgagtttaa cgtggctgtg caggtgattt caaggcatga gctgaacagc 120 gttgacacag ccgtgactta caattaaacc ctttcaatta cagtacagat tctgtgtgct 180 acttgatgag atgttaccca aggccagttt ggacttactg cttttgtccc tcatattaaa 240 ttatcaaatg atgccgatga aatgcttgaa aatgattctg ctctcaaagt tatgcttccc 300 tagaaaggtg tcatgtcggg cacttgtgtt gggtgactat gacatcccag cagtgctggt 360 caggtctcag agttgctttc acctagagct gatgcttcca caaggggaca tttgtgttac 420 tttgctccag gggtctgtca taaaaacaat ggtaactact tcatccctag gaagcccaag 480 acttcagggc actgttagct gattggtaaa taagggacac gatattcacg ggaattgttt 540 actgctcccc actagtaatt ctcatggggc cactttttta actctttcta attaacacct 600 cttctcagca tagagcagag gatgcagtca tttctctgtt gaaatctatg tagtatttat 660 gtagaatgtc attatatgaa agcgaattca gaatcctaac tctgggaaag cgctctctgg 720 aaatgtagtt tgataatagt gtcttatagg ggccacggga atttgtttct ctataaagcg 780 atgggctcca gtgtcatgtt accagagtta tcgctcagtt ttgtttgtta aggcttttgc 840 tagaacctat tatgtatcca gtttttaaaa catacttcat tcccttgata gcagagatcc 900 agagcacaga tggcaagttg tgtggatgat actgaatatg tttattttcc taaagataaa 960 tgtcacgaca cgacatttct cagtttttat ttagatgttt attaccatgt gttaacagaa 1020 tcttaaaacc caagggattt cttcagtaaa ctagactttg attcaaaaaa aaaaaaaaa 1079 <210> SEQ ID NO 214 <211> LENGTH: 103 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 214 Met Leu Pro Lys Ala Ser Leu Asp Leu Leu Leu Leu Ser Leu Ile Leu 1 5 10 15 Asn Tyr Gln Met Met Pro Met Lys Cys Leu Lys Met Ile Leu Leu Ser 20 25 30 Lys Leu Cys Phe Pro Arg Lys Val Ser Cys Arg Ala Leu Val Leu Gly 35 40 45 Asp Tyr Asp Ile Pro Ala Val Leu Val Arg Ser Gln Ser Cys Phe His 50 55 60 Leu Glu Leu Met Leu Pro Gln Gly Asp Ile Cys Val Thr Leu Leu Gln 65 70 75 80 Gly Ser Val Ile Lys Thr Met Val Thr Thr Ser Ser Leu Gly Ser Pro 85 90 95 Arg Leu Gln Gly Thr Val Ser 100 <210> SEQ ID NO 215 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 215 ggatggggct cattctctc 19 <210> SEQ ID NO 216 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 216 gaaatgtgta aactggcagc 20 <210> SEQ ID NO 217 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 217 gaatgcagca caattagagg g 21 <210> SEQ ID NO 218 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 218 ctgcttagaa agcagaattg c 21 <210> SEQ ID NO 219 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 219 tgtgactagc aatgtatgc 19 <210> SEQ ID NO 220 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 220 tcagaagaaa gccatagggc 20 <210> SEQ ID NO 221 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 221 cctcaagatg atttgcacag c 21 <210> SEQ ID NO 222 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 222 ggagagcacg ttcagaggg 19 <210> SEQ ID NO 223 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 223 gactgactct gggttcctgg 20 <210> SEQ ID NO 224 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 224 ggtagtgaag actgtgccgg 20 <210> SEQ ID NO 225 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 225 ggaagtgact tccaatgatg c 21 <210> SEQ ID NO 226 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 226 ctcgctggca ttggtttg 18 <210> SEQ ID NO 227 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 227 ccatgaccat agtcagtggg 20 <210> SEQ ID NO 228 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 228 aaatgtccaa tagttcctgg 20 <210> SEQ ID NO 229 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 229 ggagcaatgc tgagctacc 19 <210> SEQ ID NO 230 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 230 ctgcgacacc cttgacac 18 <210> SEQ ID NO 231 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 231 tcaccaagtg tatggagaat g 21 <210> SEQ ID NO 232 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 232 tatctgaacc taatggtttg 20 <210> SEQ ID NO 233 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 233 cagtcagatt tgggtcaggc 20 <210> SEQ ID NO 234 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 234 tcttacctca ggtgatccgc 20 <210> SEQ ID NO 235 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 235 gaaagccagg tcagccag 18 <210> SEQ ID NO 236 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 236 cagaggaaca cctcagaccc 20 <210> SEQ ID NO 237 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 237 ttcgtccagc agcaagtg 18 <210> SEQ ID NO 238 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 238 tatggttcgg ttgggtgg 18 <210> SEQ ID NO 239 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 239 ctacaggagg aggccgtg 18 <210> SEQ ID NO 240 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 240 ccagggaaga tgagaggaga g 21 <210> SEQ ID NO 241 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 241 gcgaaatggt ttatttactg c 21 <210> SEQ ID NO 242 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 242 cagcccttct gagtcccc 18 <210> SEQ ID NO 243 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 243 tgagagtgtg tgtgctgatt c 21 <210> SEQ ID NO 244 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 244 tccaccctcc ttgctctg 18 <210> SEQ ID NO 245 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 245 ttctcattct caagctctgc c 21 <210> SEQ ID NO 246 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 246 agaatcagag ggtcgtggg 19 <210> SEQ ID NO 247 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 247 ttgaggtatg aacagggaag g 21 <210> SEQ ID NO 248 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 248 ccaaatcatg gagaagatgc 20 <210> SEQ ID NO 249 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 249 gcccttgtat cttgggcttc 20 <210> SEQ ID NO 250 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 250 ctccacctct gcccgtag 18 <210> SEQ ID NO 251 <211> LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 251 tgggtacttt ctgcattggg 20 <210> SEQ ID NO 252 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 252 ggactaccct gttccccac 19 <210> SEQ ID NO 253 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 253 tgagcagtga ggagagagag c 21 <210> SEQ ID NO 254 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 254 gcacaaccaa cagcgctccc g 21 <210> SEQ ID NO 255 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 255 taacccaccc agacacgg 18 <210> SEQ ID NO 256 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 256 tgtctcagga ggcagaagg 19 <210> SEQ ID NO 257 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 257 aacaacatct gcatgtatcc c 21 <210> SEQ ID NO 258 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 258 agcttatcca gaccttgctt c 21 <210> SEQ ID NO 259 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 259 gtgttcttaa acacttgcat g 21 <210> SEQ ID NO 260 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 260 tgtggataca tataggaagt g 21 <210> SEQ ID NO 261 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 261 gttctcactc caggttgcg 19 <210> SEQ ID NO 262 <211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 262 tgatgagaaa agtgaaagaa c 21 <210> SEQ ID NO 263 <211> LENGTH: 19 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 263 ctgtgtagag agccagcgg 19 <210> SEQ ID NO 264 <211> LENGTH: 18 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <223> OTHER INFORMATION: oligonucleotide <400> SEQUENCE: 264 gcctcctctt ccacctcc 18 <210> SEQ ID NO 265 <211> LENGTH: 113 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 265 Met Ser Arg Pro Leu Leu Glu Arg Pro Ser Tyr Ser Leu Glu Glu Ser 1 5 10 15 Ser Pro Ala Ala Gly Phe Arg Asn Val Cys Ser Lys Leu Val Pro Ala 20 25 30 His Leu Lys Gln Ser Ser Glu Lys Val Cys Arg Asn Leu Pro Leu Pro 35 40 45 Ser Pro Ser Ser Cys Val Ala Phe Val Thr Ser Phe Leu Gln Gly Ser 50 55 60 Ser Gly Gly Gly Ser Arg Glu Ala Ala Thr Trp Leu Cys Met Trp Glu 65 70 75 80 Ser Pro Ala Ser Ser Leu His Pro His Ser Arg Thr Ala Lys Leu Gly 85 90 95 Phe Phe His Glu Glu Ala Thr Leu Met Ser Ser Leu Val Gln Leu Ser 100 105 110 Gly <210> SEQ ID NO 266 <211> LENGTH: 85 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 266 Met Ser Ser Gly Phe Leu His Thr Ser Phe Ser Trp Val Arg Leu Ala 1 5 10 15 Val Gln Ser Gly Cys Gly Gly Gly Leu Arg Arg Lys Gly His Trp Ser 20 25 30 Ser Pro Arg Phe Gly Leu Arg Gln Val His Ser Arg Tyr His Pro Thr 35 40 45 Phe Leu Ser Lys Glu Gln Ala Ser His Thr Tyr Asn Pro Phe Pro Thr 50 55 60 Leu Leu Met Tyr Pro Leu Cys Gly Thr Ser Asn Gly Gly Gln Ala Asp 65 70 75 80 Leu Pro Pro Ala Ile 85 <210> SEQ ID NO 267 <211> LENGTH: 88 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 267 Met Leu Leu Gln Ala Ser Thr Cys Asn Met Leu Thr Tyr Lys Ser Lys 1 5 10 15 Ile Ser Asp Gln Val Ala Gly Thr Ala Gly Ala Cys Gln Ala Ser Gly 20 25 30 Tyr Leu His Asp Ser Phe Pro Cys Gly Tyr Gly Arg Ala Trp Pro Phe 35 40 45 Gln Gly Ser Gln Thr Ser Tyr Thr Lys Ala Gly Leu Pro Gln Ser Gly 50 55 60 Tyr Phe Lys Gly Gly Lys Gln Lys Lys Gln His Met Tyr Asn Trp Lys 65 70 75 80 Pro Gly Gly Gly Lys Arg Gly Gln 85 <210> SEQ ID NO 268 <211> LENGTH: 59 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 268 Met Leu Gly Pro Gly Leu Cys Leu Ser Phe Gly Tyr Pro Gly Ala Ala 1 5 10 15 Pro Ala Ala Gly Pro Ala Gly Pro Gly Thr Pro Gly Pro Gly Glu Thr 20 25 30 Pro His Arg Gly Asp Pro Arg Arg Thr His Ser Val Pro Ala Ala Ala 35 40 45 Glu Ala Gln Ala Leu Gly Gly Arg Gly Phe Gly 50 55 

What is claimed is:
 1. An isolated polynucleotide which comprises the nucleotide sequence of SEQ ID NO: 9 from nucleotide 584 to nucleotide
 823. 2. An isolated polynucleotide which comprises the nucleotide sequence of a mature coding sequence of clone yc19_(—)1 deposited under accession number ATCC
 98650. 3. An isolated polynucleotide which comprises the nucleotide sequence encoding a mature protein encoded by DNA insert of clone yc19_(—)1 deposited under accession number ATCC
 98650. 